The Recall Desk

Archive

January 2024 recalls

524 recalls were announced in January 2024.

What the numbers show

Critical
12
Severe
125
High
295
Moderate
88
Low
4

Of the 524 recalls this month scored against our rubric, 2% are Critical, 24% are Severe.

101–200 of 524

  • SevereNHTSA·24V043000·2024-01-25

    PACCAR truck steering knuckles may leave axle spindles loose or fractured

    PACCAR is recalling certain 2024 Peterbilt and Kenworth trucks because bearing journals may not be fully seated in the steering knuckle assemblies. 68 units are affected.

    Product
    PETERBILT — PETERBILT, KENWORTH 520, 367, 389, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V044000·2024-01-25

    PACCAR steering gears assembled with too few recirculating balls

    PACCAR is recalling certain 2024-2025 Kenworth and Peterbilt trucks because steering gear assemblies may have fewer recirculating balls than required, risking loss of steering control.

    Product
    PETERBILT — PETERBILT, KENWORTH 579, 535, 520, L770
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V040000·2024-01-25

    Coachmen and Forest River motorhome awnings may extend during transit

    Forest River is recalling certain 2020-2023 Coachmen Galleria, Forest River Beyond and Coachmen Nova Class B motorhomes because the retractable awning may extend unintentionally during transit.

    Product
    COACHMEN — COACHMEN NOVA, GALLERIA, BEYOND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24091·2024-01-25

    Allegro Plastic Side Chairs Recalled Due to Fall Hazard

    Clark Associates is recalling about 53,800 Allegro plastic side chairs because the chairs can break apart while in use, creating a fall hazard. The company has received 16 reports of chairs breaking apart, resulting in two injuries.

    Product
    Allegro plastic side chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24E004000·2024-01-25

    Mekra Recalls Medium-Duty Vehicle Mirrors Due to Detachment Risk

    Mekra is recalling medium-duty mirrors for PACCAR vehicles because the glass lock ring may not be fully seated, allowing the mirror glass to detach.

    Product
    VISIBILITY:REARVIEW MIRRORS/DEVICES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24093·2024-01-25

    Yaomiao Children's Rhinestone Silver Tiaras Recalled for Excess Lead

    About 12,440 Yaomiao children's tiaras with rhinestones sold on Amazon.com contain lead levels that exceed federal limits. Lead is toxic if ingested by young children and can cause adverse health effects.

    Product
    Yaomiao Children's Rhinestone Silver Tiaras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24090·2024-01-25

    BRS Fuel Bottles Recalled for Non-Child-Resistant Closure Risk

    BRS Fuel Bottles sold on Amazon from December 2020 through October 2023 do not have child-resistant closures as required by law, posing a risk of burn and poisoning to children. Consumers should stop using them immediately and contact the distributor for return or disposal.

    Product
    BRS Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24094·2024-01-25

    Visual Comfort Maverick Coastal Outdoor Ceiling Fans Impact Injury Recall

    Visual Comfort & Co. is recalling Maverick Coastal 60-inch outdoor ceiling fans because the blades can crack or break and fall, posing an impact injury hazard. The manufacturer has received nine reports of blade failure but no injuries or property damage so far.

    Product
    Maverick Coastal 60-inch Outdoor Ceiling Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0762-2024·2024-01-24

    Herold's Salad Shell Macaroni Salad Recalled for Potential Listeria Contamination

    Herold Salads, Inc. is recalling Herold's Salad Shell Macaroni Salad in 1lb, 2lb, and 5lb containers due to potential Listeria monocytogenes contamination. The affected product was distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salad - Shell Macaroni Salad packaged in 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0743-2024·2024-01-24

    Herold's Black Bean and Corn Salsa recalled for potential Listeria contamination

    Herold Salads, Inc. is recalling Black Bean and Corn Salsa due to potential contamination with Listeria monocytogenes. Affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salads - Black Bean and Corn Salsa packaged in 12oz, 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Devices)·Z-0620-2024·2024-01-24

    Surgical Convenience Kit Recalled Due to Defective Component

    ROi CPS LLC is recalling 345 units of regard Operative LAP surgical convenience kits distributed in Louisiana because they were manufactured with a component that was subsequently recalled by Nurse Assist.

    Product
    regard Operative LAP, Item Number 800943001; surgical convenience kit
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Food)·F-0737-2024·2024-01-24

    Herold's Salads Potato Salad Recalled Due to Listeria Risk

    Herold Salads, Inc. is recalling potato salad products in 1lb, 2lb, 5lb, and 10lb tubs due to potential Listeria monocytogenes contamination. The recall affects products distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salads -Potato Salad packaged in 1lb, 2lb, 5lb, and 10lb plastic tubs.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0758-2024·2024-01-24

    Herold's Salads Rainbow Rotini Recalled for Potential Listeria Contamination

    Herold Salads is recalling Rainbow Rotini salad packages in 1lb, 2lb, and 5lb sizes due to potential contamination with Listeria monocytogenes. The affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salads - Rainbow Rotini packaged in 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0755-2024·2024-01-24

    Herold's Potato Salad recalled for potential Listeria monocytogenes contamination

    Herold's Original Potato Salad with egg is being recalled due to potential contamination with Listeria monocytogenes. The product was distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salad - Original Potato Salad with egg packaged in 8oz, 1lb, 2lb, 5lb, and 10lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0240-2024·2024-01-24

    Old Spice Sweat Defense Spray Recalled for Benzene Contamination Nationwide

    Old Spice Sweat Defense Pure Sport Plus anti-perspirant spray is being recalled nationwide due to benzene contamination in specific lot numbers. Consumers should discontinue use of affected products immediately.

    Product
    Old Spice, SWEAT DEFENSE PURE SPORT PLUS, Dry Spray, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical spray can, Net WT 3.8 oz (107 g) cans, Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-387-10, UPC 0 37000 72974 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0241-2024·2024-01-24

    Old Spice Anti-Perspirant Spray Recalled Due to Benzene Contamination

    Old Spice Sweat Defense Ultimate Captain anti-perspirant spray is being recalled due to benzene contamination. The FDA Class I recall affects products distributed nationwide and internationally.

    Product
    Old Spice, SWEAT DEFENSE ULTIMATE CAPTAIN, Aluminum Chlorohydrate 23.5%, Anti-Perspirant, Topical spray can 3.8 OZ (107 g), Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-385-10, UPC 0 37000 74947 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0769-2024·2024-01-24

    Natures Wonder Premium Bean Sprouts Recalled Due to Listeria

    Natures Wonder Premium Bean Sprouts are being recalled due to Listeria monocytogenes contamination. The recalled product was distributed in Massachusetts, Connecticut, New York, and Maryland.

    Product
    Natures Wonder Premium Bean Sprouts
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0768-2024·2024-01-24

    Amish Wedding Potato Salad Recalled for Potential Listeria Contamination

    Herold Salads, Inc. recalls Amish Wedding Southern Potato Salad with egg due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Amish Wedding - Southern Potato Salad with egg packaged in 12oz, 1lb, 2lb, 3lb, 5lb, and 10b plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0745-2024·2024-01-24

    Herold's Salads Crab Dip Recalled Due to Listeria Contamination Risk

    Herold's Salads is recalling crab dip sold in Ohio, Pennsylvania, and Michigan due to potential Listeria monocytogenes contamination. Affected products expire 11/29/23 or 12/12/23.

    Product
    Herold's Salads - Crab Dip packaged in 12oz, 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0715-2024·2024-01-24

    Spinach Pie Products Recalled Due to Undeclared Allergens

    NBRBDR Inc. is recalling spinach pie products with best-by dates from November 17 to December 15, 2023, due to undeclared allergens: egg, milk, and wheat. Products were distributed in California.

    Product
    SPINACH PIE (2 oz)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0763-2024·2024-01-24

    Cleveland's Own Shell Macaroni Salad Recalled for Listeria Contamination Risk

    Herold Salads, Inc. is recalling Cleveland's Own Shell Macaroni Salad due to potential Listeria monocytogenes contamination. The affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Cleveland's Own - Shell Macaroni Salad packaged in 10b plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0637-2024·2024-01-24

    Breathing Circuit Kits Recalled Due to Assembly Error Affecting Pressure

    Percussionaire Corporation is recalling High Frequency Transport Phasitron Breathing Circuit Kits due to assembly errors that can affect pressure output. The defect could impact respiratory support to patients using this device.

    Product
    High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123
    Category
    Medical Device
    Distribution
    21 states
  • SevereFDA (Drugs)·D-0235-2024·2024-01-24

    Atropine Sulfate Injection Recalled for Glass Particulate Matter Contamination

    Pfizer Inc. is recalling Atropine Sulfate Injection due to glass particulate matter contamination in lot GY2496. This FDA Class I recall affects 24,400 cartons distributed nationwide in the USA and Puerto Rico.

    Product
    ATROPINE SULFATE — ATROPINE SULFATE (ATROPINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0739-2024·2024-01-24

    Potato Salad Recalled for Potential Listeria Contamination

    Herold Salads, Inc. is recalling Amish Wedding Potato Salad due to potential Listeria monocytogenes contamination. The affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Amish Wedding -Potato Salad packaged in 12oz and 5lb plastic tubs.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0234-2024·2024-01-24

    FDA Recalls Sodium Bicarbonate Injection Due to Glass Particle Contamination

    Pfizer Inc. is recalling 21,200 cartons of Sodium Bicarbonate Injection (lot HA7295, expiring March 1, 2025) nationwide due to glass particle contamination. The product is distributed in the United States and Puerto Rico.

    Product
    SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0761-2024·2024-01-24

    Herold's Salad Santa Fe Pasta Recalled for Potential Listeria Contamination

    Herold Salads, Inc. is recalling Herold's Salad Santa Fe Pasta sold in 1lb, 2lb, and 5lb containers from Ohio, Pennsylvania, and Michigan due to potential Listeria monocytogenes contamination.

    Product
    Herold's Salad - Santa Fe Pasta packaged in 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0759-2024·2024-01-24

    Herold's Rotini Garden Medley Salad Recalled for Listeria Contamination Risk

    Herold Salads is recalling Rotini Garden Medley packaged salad due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salads - Rotini Garden Medley packaged in 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0741-2024·2024-01-24

    Dutch Valley Macaroni Salad recalled for potential Listeria contamination

    Dutch Valley Macaroni Salad sold in Ohio, Pennsylvania, and Michigan may be contaminated with Listeria monocytogenes. The recalled products include 1lb, 2lb, 5lb, and 10lb tubs distributed by Herold Salads, Inc.

    Product
    Dutch Valley -Macaroni Salad packaged in 1lb, 2lb, 5lb, and 10lb plastic tubs.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0710-2024·2024-01-24

    FDA Recalls Express Chest Drain Blood Recovery Units Over Infection Risk

    Maquet Cardiovascular is recalling Express chest drain units with defective sterile water syringes. If not kept upright, patients risk exposure to infectious material that may cause infection, abscess, sepsis, or death.

    Product
    Product REF 4050-100N, DRAIN, EXPRESS BRU W/AC, Blood Recovery Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0693-2024·2024-01-24

    Percussionaire Distal Phasitron respiratory device with reservoir bag assembly defect recalled

    Percussionaire Corporation recalled 195 Distal Phasitron devices after finding the breathing circuit reservoir bag may be assembled at the wrong attachment point, potentially affecting therapy delivery.

    Product
    Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Food)·F-0742-2024·2024-01-24

    Amish Wedding Macaroni Salad Recalled Due to Listeria Contamination Risk

    Herold Salads, Inc. is recalling Amish wedding Macaroni Salad due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Amish wedding -Macaroni Salad packaged in 12oz, 1lb, 5lb, and 10lb plastic tubs.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0243-2024·2024-01-24

    Secret Dry Spray Antiperspirant recalled due to benzene contamination

    The FDA has recalled Secret Dry Spray Antiperspirant due to benzene contamination in certain lots. Affected products were distributed nationwide in the USA, Puerto Rico, Canada, and internationally.

    Product
    Secret, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Waterlily, Topical Spray Can, Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-381-10; UPC 0 37000 72372 1; 12/pack UPC 0 37000 72991 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0238-2024·2024-01-24

    Old Spice PURE SPORT Anti-Perspirant Spray Recalled for Benzene Contamination

    Old Spice PURE SPORT Anti-Perspirant Spray is recalled for benzene contamination in certain lot numbers. The product was distributed nationwide and internationally.

    Product
    Old Spice, PURE SPORT, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant & Deodorant Spray, Topical spray can, Net WT 6.0 OZ (170g), Distributed by Procter & Gamble, Cincinnati, OH 45202. NDC: 37000-199-60, UPC 0 12044 00191 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0760-2024·2024-01-24

    Amish Wedding Rotini Garden Medley Recalled for Listeria Contamination

    Herold Salads, Inc. is recalling Amish Wedding Rotini Garden Medley due to potential Listeria monocytogenes contamination. The product was distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Amish Wedding - Rotini Garden Medley packaged in 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0246-2024·2024-01-24

    Secret Dry Spray Antiperspirant Recalled for Benzene Contamination

    The FDA is recalling Secret Dry Spray antiperspirant (Lot #12001458SF) due to benzene contamination. Consumers should stop using the product immediately.

    Product
    Secret, Dry Spray, Aluminum chlorohydrate 23.5%, Antiperspirant, Rose, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-380-10, UPC 0 37000 79884 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0233-2024·2024-01-24

    Sodium Bicarbonate Injection recalled for glass particulate contamination

    Pfizer is recalling 34,000 cartons of 4.2% Sodium Bicarbonate Injection nationwide due to glass particles in the solution. Patients should immediately stop use and contact their supplier.

    Product
    4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake Forst, IL 60045, NDC 0409-5534-24 (carton), 0409-5534-14 (case).
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0236-2024·2024-01-24

    Topical Drug Recalled: Americaine Benzocaine Spray Contaminated with Benzene

    Americaine benzocaine 20% topical anesthetic spray is being recalled nationwide due to benzene chemical contamination. The recall affects 34,704 cans with lot number 1A16420 and expiration date 01/31/2025.

    Product
    AMERICAINE — AMERICAINE (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0746-2024·2024-01-24

    Amish Wedding Cucumber Salad Recalled for Listeria Contamination Risk

    Herold Salads is recalling Amish Wedding Cucumber Salad products sold in Ohio, Pennsylvania, and Michigan due to potential Listeria monocytogenes contamination. Affected lot codes have been identified by the FDA.

    Product
    Amish Wedding - Cucumber Salad packaged in 12oz, 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0767-2024·2024-01-24

    Herold's Salads Southern Potato Salad Recalled for Listeria Contamination

    Herold's Salads Southern Potato Salad with egg is being recalled due to potential Listeria monocytogenes contamination. The recall affects products distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salads - Southern Potato Salad with egg packaged in 12oz, 1lb, 2lb, 3lb, 5lb, and 10b plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0714-2024·2024-01-24

    Spanakopita recalled for undeclared allergens: eggs, milk, soy

    Nutritious Delicious Foods is recalling spanakopita pastries sold in California because they contain undeclared eggs, milk, and soy allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    Spanakopita, 6 oz (3 oz each piece), in plastic clam shell container
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0721-2024·2024-01-24

    Quaker Oats Chewy Granola Bars recalled due to potential Salmonella contamination

    Houdini Inc. is recalling Ministry of Snacks Sweet and Savory Collection #8700 gift baskets containing Quaker Oats Chewy Granola Bars due to potential Salmonella contamination. The recall affects 926 units distributed nationwide.

    Product
    Ministry of Snacks Sweet and Savory Collection #8700
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0764-2024·2024-01-24

    Herold's Southern Macaroni Salad recalled due to Listeria contamination risk

    Herold Salads, Inc. is recalling its Southern Macaroni Salad sold in Ohio, Pennsylvania, and Michigan due to potential Listeria monocytogenes contamination. Affected products carry expiration dates from December 4, 2023 through January 15, 2024.

    Product
    Herold's Salad - Southern Macaroni Salad packaged in 1lb, 2lb, 3lb, 5lb, and 10b plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0748-2024·2024-01-24

    Herold's Salads Health Salad recalled for potential Listeria contamination

    Herold Salads, Inc. is recalling Health Salad products distributed in Ohio, Pennsylvania, and Michigan due to potential contamination with Listeria monocytogenes.

    Product
    Herold's Salads - Health Salad packaged in 12oz, 1lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0753-2024·2024-01-24

    Herold's Salad Poppyseed Bowtie Pasta Recalled for Potential Listeria Contamination

    Herold Salads is recalling poppyseed bowtie pasta due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salad - Poppyseed Bowtie Pasta packaged in 1lb, 2lb, 3lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0756-2024·2024-01-24

    Cleveland's Own Potato Salad Recalled for Potential Listeria Contamination

    Herold Salads, Inc. is recalling Cleveland's Own - Original Potato Salad due to potential Listeria monocytogenes contamination. The affected product was distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Cleveland's Own - Original Potato Salad packaged in 10lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0740-2024·2024-01-24

    Herold's Macaroni Salad Recalled for Listeria Contamination Risk

    Herold Salads, Inc. is recalling Herold's Macaroni Salad in 1lb to 10lb tubs due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salad -Macaroni Salad packaged in 1lb, 2lb, 5lb, and 10lb plastic tubs.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0719-2024·2024-01-24

    Assorted 2 oz Pies Recalled for Undeclared Allergens

    Nutritious Delicious Foods is recalling assorted 2 oz pies distributed in California for undeclared egg, milk, and wheat allergens.

    Product
    ASSORTED 2 OZ PIES - Cheese, Spinach, Zucchini Mushroom (12 oz)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0771-2024·2024-01-24

    Spinach Recalled Due to Listeria monocytogenes Contamination

    Fresh Express and Publix spinach products are being recalled due to Listeria monocytogenes contamination confirmed by the Florida Department of Agriculture. The products were distributed to seven southeastern states.

    Product
    Spinach sold under the brand names of Fresh Express NET WT. 8 OZ (227G) UPC 0 71279 13204 4 FRESH EXPRESS INCORPORATED PO BOX 80399, SALINAS, CA 93912 & Publix NET WT 9 OZ (255g) UPC 0 41415 00886 1 DISTRIBUTED BY PUBLIX SUPER MARKETS, INC., LAKELAND, FL 33802
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0750-2024·2024-01-24

    Herold's Macaroni Salad Recalled for Potential Listeria Contamination

    Herold Salads is recalling macaroni salad in multiple sizes due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salad - Macaroni Salad (Elbow) packaged in 8oz, 12oz, 1lb, 2lb, 5lb, and 10lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0242-2024·2024-01-24

    Secret Powder Fresh Antiperspirant Spray Recalled for Benzene Contamination

    The Procter & Gamble Company is recalling Secret antiperspirant/deodorant spray due to the presence of benzene, a chemical contaminant. The recall affects multiple lot numbers distributed nationwide and internationally.

    Product
    SECRET ANTIPERSPIRANT — SECRET ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0757-2024·2024-01-24

    Corky's & Lenny's Potato Salad Recalled for Listeria monocytogenes

    Herold Salads, Inc. is recalling Corky's & Lenny's potato salad packaged in 30-pound containers due to potential Listeria monocytogenes contamination. Affected products were distributed to Ohio, Pennsylvania, and Michigan.

    Product
    Corky's & Lenny's - Potato Salad packaged in 30lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0772-2024·2024-01-24

    Fresh-cut fruit and cantaloupe products recalled for potential Salmonella contamination

    CF Dallas LLC is recalling fresh-cut fruit products because they were made from cantaloupe potentially contaminated with Salmonella. The 27,998 units affected were distributed to retailers in ten states.

    Product
    Seasonal Blend 10oz, Seasonal Blend 16oz, Seasonal Blend 42oz , Melon Trio 16oz, Melon Mix 32oz, Fruit Blend 16oz, Fruit Bowl 40oz, Seasonal Fruit Tray 48oz, Fruit Mix 32oz, Cantaloupe Chunks 10oz, Cantaloupe Chunks 16oz, Fruit Medley 6oz- all packaged in clear plastic clamshells
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0749-2024·2024-01-24

    Herold's Salads Lemon Spring Rotini recalled for potential Listeria contamination

    Herold Salads, Inc. is recalling Lemon Spring Rotini packaged in 1lb, 2lb, and 5lb containers due to potential Listeria monocytogenes contamination. The affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salads - Lemon Spring Rotini packaged in 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0809-2024·2024-01-24

    Enfamil Nutramigen Infant Formula Recalled for Potential Cronobacter Contamination

    Mead Johnson is recalling Enfamil Nutramigen Hypoallergenic Infant Formula Powder due to potential Cronobacter sakazakii contamination. Approximately 1.4 million cans with specific UPC codes (300871239418 or 300871239456) and January 1, 2025 use-by date are affected.

    Product
    Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6 OZ and 19.8 OZ). UPC Code of 300871239418 or 300871239456 and Use By Date of "1 Jan 2025".
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0718-2024·2024-01-24

    Zucchini Mushroom Pie Recalled for Undeclared Egg, Milk, Wheat Allergens

    NBRBDR Inc. is recalling Zucchini Mushroom Pie (5 oz) due to undeclared allergens: egg, milk, and wheat. Consumers with allergies to these ingredients should not consume the product.

    Product
    Zucchini Mushroom PIE (5 oz)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0738-2024·2024-01-24

    Dutch Valley Potato Salad recalled due to Listeria contamination risk

    Herold Salads, Inc. is recalling Dutch Valley Potato Salad products due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Dutch Valley -Potato Salad packaged in 1lb, 2lb, 5lb, and 10lb plastic tubs.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0766-2024·2024-01-24

    Herold's Salads Southern Potato Salad Recalled Due to Listeria Risk

    Herold Salads is recalling Southern Potato Salad in multiple sizes sold in Ohio, Pennsylvania, and Michigan due to potential Listeria monocytogenes contamination. Consumers should not consume affected products.

    Product
    Herold's Salads - Southern Potato Salad packaged in 12oz, 1lb, 2lb, 3lb, 5lb, and 10b plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0717-2024·2024-01-24

    Spinach Feta Pie Recalled for Undeclared Allergens: Egg, Milk, Wheat

    NBRBDR Inc. is recalling its 5-ounce Spinach Feta Pie because it contains undeclared allergens: egg, milk, and wheat. Consumers with allergies to these ingredients should not consume the product.

    Product
    SPINACH FETA PIE (5 oz)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0716-2024·2024-01-24

    Cheese Pies Recalled for Undeclared Egg, Milk, and Wheat Allergens

    NBRBDR Inc. is recalling cheese pies distributed in California due to undeclared allergens: egg, milk, and wheat. Consumers with allergies to these ingredients should not consume the product.

    Product
    CHEESE PIE (5 oz)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0751-2024·2024-01-24

    Cleveland's Own Macaroni Salad Recalled for Potential Listeria Contamination

    Cleveland's Own Macaroni Salad sold in 5-pound and 10-pound containers is being recalled due to potential Listeria monocytogenes contamination. The recall affects products distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Cleveland's Own - Macaroni Salad (Elbow) - packaged in 5lb and 10lb plastic containers
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0709-2024·2024-01-24

    Express Chest Drains Recalled for Infection Risk from Recalled Syringes

    Maquet Cardiovascular is recalling Express chest drains pre-packaged with recalled sterile water syringes. If not kept upright, patients may be exposed to infectious material, risking infection, abscess, sepsis, and death.

    Product
    Product REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single Collection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0770-2024·2024-01-24

    Fresh Express Lettuce Recalled for Listeria monocytogenes Contamination

    Fresh Express 2-pound bags of lettuce distributed across seven southern states have been recalled due to Listeria monocytogenes contamination confirmed by the Florida Department of Agriculture.

    Product
    Lettuce in clear plastic 2lb bags.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0244-2024·2024-01-24

    Secret Dry Spray Antiperspirant Recalled Due to Benzene Contamination

    Procter & Gamble is recalling Secret Dry Spray Antiperspirant due to benzene contamination in specific lot numbers. The FDA has classified this as a Class I recall.

    Product
    Secret, Dry Spray, Aluminum chlorohydrate 23.5%, Antiperspirant, Lavender, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-383-10, UPC: 0 37000 72986 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0747-2024·2024-01-24

    Herold's Salads Greek Gemelli Pasta Salad Recalled for Listeria Risk

    Herold Salads, Inc. is recalling Greek Gemelli Pasta Salad due to potential Listeria monocytogenes contamination. The recall affects products distributed in Ohio, Pennsylvania, and Michigan.

    Product
    Herold's Salads - Greek Gemelli Pasta Salad packaged in 12oz, 1lb, 2lb, and 5lb plastic containers
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0245-2024·2024-01-24

    Secret Dry Spray Antiperspirant recalled due to potential benzene contamination

    Procter & Gamble is recalling Secret Dry Spray Antiperspirant due to potential benzene contamination from manufacturing facility issues. No illnesses have been reported.

    Product
    Secret, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Light Essentials, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-382-10, UPC 0 37000 72992 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0256-2024·2024-01-24

    Secret Dry Spray Antiperspirant Recalled Over Manufacturing Facility Defect

    Secret Dry Spray antiperspirant is being recalled due to CGMP violations at the manufacturing facility where other lots were found contaminated with benzene. No illnesses have been reported.

    Product
    Secret Dry Spray, Aluminum chlorohydrate 23.5%, Antiperspirant, Rose, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-380-10, UPC 0 37000 79884 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0249-2024·2024-01-24

    Old Spice Pure Sport Gift Set Recalled for Benzene Contamination Risk

    Procter & Gamble is recalling Old Spice Pure Sport 2021 Gift Sets due to benzene contamination at the manufacturing facility. No illnesses have been reported.

    Product
    Old Spice Pure Sport 2021 Gift Set, Contains: Old Spice Pure Sport Body Wash 18 Fl Oz (532 mL), 2-in-1 Shampoo & Conditioner 13.5 Fl Oz (400 mL), and Old Spice, SWEAT DEFENSE PURE SPORT PLUS, Dry Spray, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical spray can, Net WT
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0254-2024·2024-01-24

    Secret Dry Spray Antiperspirant Recalled for Potential Benzene Contamination

    The FDA has recalled Secret Dry Spray Antiperspirant in Waterlily scent due to potential benzene contamination at the manufacturing facility. All lots with expiration dates through September 2023 are affected.

    Product
    Secret, Dry Spray, Aluminum chlorohydrate 23.5% Antiperspirant, Waterlily, Topical Spray Can, Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-381-10; UPC 0 37000 72372 1; 12/pack UPC 0 37000 72991 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0738-2024·2024-01-24

    COVID-19 Rapid Antigen Test Recalled for Incorrect Expiration Date Labeling

    INDICAID COVID-19 Rapid Antigen At-Home Tests were released with an incorrect expiration date (05 April 2024) instead of the correct date (21 February 2024). Expired tests may produce inaccurate or invalid results.

    Product
    INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0250-2024·2024-01-24

    Old Spice Pure Sport Deodorant Spray Recalled for Benzene Contamination Risk

    Procter & Gamble is recalling Old Spice Pure Sport Anti-Perspirant & Deodorant Spray (6.0 oz) due to potential benzene contamination risk from manufacturing facility CGMP deviations. All affected lots expire through September 2023.

    Product
    Old Spice, PURE SPORT, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant & Deodorant Spray, Topical spray can, Net WT 6.0 OZ (170g), Distributed by Procter & Gamble, Cincinnati, OH 45202. NDC: 37000-199-60, UPC 0 12044 00191 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0251-2024·2024-01-24

    Old Spice Anti-Perspirant Spray Recalled for Potential Benzene Contamination

    The FDA has recalled Old Spice SWEAT DEFENSE PURE SPORT PLUS anti-perspirant spray due to potential benzene contamination found at the manufacturing facility. All lots through September 2023 are affected.

    Product
    Old Spice, SWEAT DEFENSE PURE SPORT PLUS, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical spray can, Net WT 3.8 oz (107 g) cans, Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-387-10, UPC 0 37000 72974 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0239-2024·2024-01-24

    Old Spice Anti-Perspirant Spray Recalled Due to Facility Benzene Contamination

    Old Spice SWEAT DEFENSE Dry Spray anti-perspirant is being recalled due to manufacturing facility issues where other product lots were found contaminated with benzene. No illnesses have been reported.

    Product
    Old Spice, SWEAT DEFENSE, STRONGER SWAGGER, Dry Spray, 48 Hour, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical Spray Can, Net WT 3.8 oz (107 g), Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC 69423-386-10, UPC 0 37000 73034 7 OR UPC 0 12044 04475 9 (12 Pack, ol
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0248-2024·2024-01-24

    Secret OUTLAST Dry Spray Antiperspirant Recalled for Benzene Contamination

    Procter & Gamble is recalling Secret OUTLAST Dry Spray antiperspirant (3.8 oz) due to potential benzene contamination at the manufacturing facility. All lots expiring through September 2023 are affected.

    Product
    Secret OUTLAST Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Protecting Powder, Topical spray can 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-478-10, UPC 0 37000 74772 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0253-2024·2024-01-24

    Secret anti-perspirant spray recalled for potential benzene contamination

    The FDA is recalling Secret powder fresh anti-perspirant spray due to potential benzene contamination found at the manufacturing facility.

    Product
    SECRET ANTIPERSPIRANT — SECRET ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0734-2024·2024-01-24

    FreeStyle Libre 3 App may lose signal on Android 13 devices

    Abbott is recalling FreeStyle Libre 3 App on Android 13 devices due to signal loss that may prevent users from receiving glucose readings and alarms, potentially delaying necessary treatment.

    Product
    FreeStyle Libre 3 App, part of Continuous Glucose Monitoring System, when used on the Android 13 Operating System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0247-2024·2024-01-24

    Secret OUTLAST Dry Spray Antiperspirant recalled for potential benzene contamination

    Procter & Gamble is recalling Secret OUTLAST Dry Spray Antiperspirant due to a manufacturing facility deviation where other lots were found contaminated with benzene. The recalled product was manufactured at the affected facility.

    Product
    Secret, OUTLAST, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Completely Clean, Topical spray can 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-384-10, UPC 0 37000 74764 2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0766-2024·2024-01-24

    Maquet XTen OR Light Systems Recalled for Potential Fall Hazard

    The FDA is recalling multiple Maquet XTen OR Light System models because they may unexpectedly fall in the operating room. The recall affects 236,793 units distributed nationwide and globally.

    Product
    Maquet XTen OR Light Systems, Model Numbers and Catalog Numbers 3001 HMD14 - ARD567732001C, X TEN DUO - ARD568221510C, X TEN DUO - ARD568221561C, X10AXL DF - ARD568211010C, X10AXL SF - ARD568231010C, X10AXL+ DF - ARD568211710C, X10AXLDUO - ARD568211000C, X10DF - ARD568211110C, X1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0725-2024·2024-01-24

    Central Market Organic Chicken Broth Concentrate Recalled for Microbial Contamination

    TreeHouse Foods, Inc. is recalling Central Market 16oz Organic Low Sodium Chicken Broth Concentrate due to potential microbial contamination. The affected product has been distributed to 41 states.

    Product
    Central Market 16oz Organic Low Sodium Chicken Broth Concentrate
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-0720-2024·2024-01-24

    Member's Mark Mild Cheddar Shredded Cheese Recalled for Glove Remnants

    Member's Mark Mild Cheddar shredded cheese is being recalled due to possible glove remnants. The recall affects specific lots distributed to Illinois, Indiana, Missouri, and Ohio.

    Product
    Member's Mark - Mild Cheddar Fancy (Fine) Shredded Cheese packaged in 5lbs, 8 packages per case
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0755-2024·2024-01-24

    Suction Canister Liners Recalled for Potential Loss of Suction Function

    Cardinal Health suction canister liners may lose suction on low settings due to liner misalignment. Approximately 203,244 units distributed to the US, Canada, Australia, and New Zealand.

    Product
    Cardinal Health MEDI-VAC CRD Suction Canister Liner, 1000 mL Suction Canister Liner Kit with 5 mm 1.8 m Tube, REF 65651-516
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0749-2024·2024-01-24

    Link Patella Glide Resection Guide recalled due to size mislabeling

    A surgical guide used in knee replacement is recalled due to mislabeling showing incorrect dimensions. This could result in improper bone resection and implant fit, potentially extending surgery time.

    Product
    Link Patella Glide Resection Guide- For the implantation of the Endo-Model Knee System as part of a total knee arthroplasty procedure. Product Code: 15-2530/05
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0227-2024·2024-01-24

    Magnesium Citrate Laxative Oral Solution Recalled for Bacterial Contamination

    Good Neighbor Pharmacy brand Magnesium Citrate laxative is being recalled due to Acetobacter nitrogenifigens bacterial contamination. The FDA recommends consumers stop using the product.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (MAGNESIUM CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0231-2024·2024-01-24

    Magnesium Citrate Oral Solution Recalled for Bacterial Contamination

    Pharma Nobis LLC is recalling 7,404 bottles of Freskaro Magnesium Citrate Oral Solution nationwide due to the presence of Acetobacter nitrogenifigens bacteria.

    Product
    MAGNESIUM CITRATE — MAGNESIUM CITRATE (FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - CHERRY)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0763-2024·2024-01-24

    Maquet PowerLED and PowerLED300 Surgical Light Systems Fall Hazard Recall

    Getinge recalls 236,793 units of Maquet PowerLED and PowerLED300 operating room light systems due to a potential for the light to fall in the operating room.

    Product
    Maquet PowerLED/HLED and PowerLED300 OR Light Systems, Model Numbers and Catalog Numbers EPS MB1 - ARDINT059002A, EPS MB1 - ARDINT059002C, EPS MB1 TR - ARDINT059000A, EPS MB1 TR - ARDINT059000C, EPS MB3 - ARDINT059003A, EPS MB3 - ARDINT059003C, EPS MB3 TR - ARDINT059001A, EPS MB3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0752-2024·2024-01-24

    Medical Diagnostic Calibration Serum Recalled for Positive Measurement Bias

    Randox Laboratories is recalling Calibration Serum Level 3 (CAL2351) distributed in the US and Puerto Rico because it exhibits a positive bias in CK Total measurements on RX Series instruments, potentially affecting test accuracy by up to 13%.

    Product
    Calibration Serum Level 3 CAL2351
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0718-2024·2024-01-24

    SOLTIVE SuperPulsed Laser Fibers May Have Breached Sterile Pouch Seals

    Olympus Corporation recalls 179 SOLTIVE SuperPulsed Laser Fibers due to potentially breached sterile pouch seals that could cause procedure delays or patient infections if not detected before use.

    Product
    SOLTIVE SuperPulsed Laser Fibers, Model No. TFL-FBX200BS
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Devices)·Z-0642-2024·2024-01-24

    ExcelsiusGPS surgical navigation system calibration error may cause device misplacement

    Globus Medical is recalling the ExcelsiusGPS Flat Panel Fluoroscopy Fixture Kit due to a calibration error that may cause inaccurate navigation and device misplacement during surgery. Nine units are distributed across select US states and internationally.

    Product
    ExcelsiusGPS Flat Panel Fluoroscopy Fixture Kit, Part number 6203.2100
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0740-2024·2024-01-24

    Medical Device Stopcock Recalled Due to O-Ring Seal Defect

    Smiths Medical Asd Inc is recalling approximately 31,685 Stopcock Left Rotator devices due to oversized O-rings that may compromise seal integrity. The defect may cause medication leaks, potentially resulting in under-infusion during treatment.

    Product
    1050 STOPCOCK LEFT ROTATOR OFF HANDLE, List Number MX1431MRL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0728-2024·2024-01-24

    Ultrasound Examination Table Recall Due to Backrest Platform Stress Fracture

    Oakworks Inc is recalling Ultrasound EA examination tables because the backrest platform can develop stress fractures, making the table inoperable in inclined positions. Approximately 104 units distributed nationwide are affected.

    Product
    Ultrasound EA (Ergonomic Advantage) table versions; G3 (General 3 Section) Echocardiography -An Ultrasound examination table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0750-2024·2024-01-24

    GammaPod Radiation Treatment Planning System Software Error Allows Wrong Imaging Structures

    Xcision Medical Systems recalled 4 GammaPod Treatment Planning Systems due to a software error that allows incorrect radiation structures from previous CT scans to be imported and selected, potentially affecting treatment planning accuracy.

    Product
    GammaPod - Treatment Planning System-a component of the GammaPod Irradiation System. Ref: XMSGP030A09.07-0.01 Intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0735-2024·2024-01-24

    Intraocular Lens Cylinder Axis Marks Out of Specification

    Johnson & Johnson is recalling TECNIS Toric II intraocular lenses distributed in Japan. The cylinder axis marks do not meet product specifications and could affect vision correction.

    Product
    TECNIS Toric II OptiBlue IOL Models ZCW
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0757-2024·2024-01-24

    Maquet PowerLEDII Operating Room Light System Recalled for Fall Risk

    Getinge Usa Sales Inc is recalling Maquet PowerLEDII OR light systems due to a potential for the light to fall in the operating room. No injuries have been reported.

    Product
    Maquet PowerLEDII OR Light System, Model Names and Catalog Numbers PWDII77SF - ARDPWT629100A, PWDII555DF - ARDPWT629101A, PWDII555SF - ARDPWT629102A, PWDII755DF - ARDPWT629103A, PWDII755SF - ARDPWT629104A, PWDII775DF - ARDPWT629105A, PWDII775SF - ARDPWT629106A, PWDII50DF - ARDPWT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0713-2024·2024-01-24

    Deli Carolina Style Mustard BBQ Sauce recalled for undeclared fish allergen

    Ventura Foods is recalling Deli Carolina Style Mustard BBQ Sauce for undeclared fish (anchovy) allergen. If you have a fish allergy, do not consume this product.

    Product
    DELI CAROLINA STYLE MUSTARD BBQ SAUCE, 2 oz (57g), plastic cup, 96 cups/case, store in ambient temperatures
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0769-2024·2024-01-24

    Maquet G8 Operating Room Light Systems Recalled for Fall Risk

    Getinge USA is recalling Maquet G8 and G8E operating room light systems that may fall during use. Approximately 236,793 units have been distributed nationwide and globally.

    Product
    Maquet G8 / G8E OR Light Systems, Model Numbers and Catalog Numbers G8 LC E - ARD568131211C, G8G8 DF E - ARD568121111C, G8G8FS DF - ARD568121131C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0768-2024·2024-01-24

    Maquet Hanaulux HLX2000 Operating Room Lights Recalled Due to Fall Hazard

    Getinge Usa Sales Inc is recalling Maquet Hanaulux HLX2000 OR Light Systems because the light fixture may fall from its mounting in the operating room. Nearly 237,000 units are affected.

    Product
    Maquet Hanaulux HLX2000 OR Light Systems, Model Numbers and Catalog Numbers 3001 - ARD567424001C, 3001 HMS07 - ARD567722001C, 3001 HXS12 - ARD567703001C, 4001 S/DF - ARD567211211C, 4001 SAD/DF - ARD567221211C, 4001 SAD/DF - ARD567221241C, 4001 SAD/SF - ARD567221141C, 4001 SAI/DF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0761-2024·2024-01-24

    Maquet Operating Room Light Systems Recalled Due to Fall Risk

    Getinge USA Sales Inc is recalling Maquet Equipment OR Light Systems due to a potential risk that the light systems could fall in the operating room. Approximately 236,793 units have been distributed.

    Product
    Maquet Equipment OR Light Systems, Model Numbers and Catalog Numbers BRAINLAB CAMERA - ARDEQT269000A, BRAINLAB CAMERA - ARDEQT269000C, BRAINLAB CAMERA - ARDEQT269001A, BRAINLAB CAMERA - ARDEQT269001C, BRAINLAB CAMERA - ARDEQT269004A, BRAINLAB CAMERA - ARDEQT269004C, BRAINLAB CAME
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0742-2024·2024-01-24

    Medex 700PSI Stopcock with Rotator Recalled Due to Seal Defect

    Smiths Medical is recalling Medex 700PSI stopcocks with rotators due to a manufacturing defect affecting the O-ring seal. The defect may cause medication leakage and under-infusion during patient treatment.

    Product
    Medex 700PSI STOPCOCK W/ROTATOR, List Number MX4331R
    Category
    Medical Device
    Distribution
    Distributed nationwide

Looking for a different month? Back to 2024.