The Recall Desk

Archive

June 2024 recalls

526 recalls were announced in June 2024.

What the numbers show

Critical
17
Severe
130
High
341
Moderate
34
Low
4

Of the 526 recalls this month scored against our rubric, 3% are Critical, 25% are Severe.

Which agencies issued them

1–100 of 526

  • SevereUSDA FSIS·019-2024·2024-06-30

    Michael Foods Recalls Liquid Egg Products Due to Undeclared Milk Allergen

    Michael Foods is recalling approximately 4,620 pounds of liquid egg products because they contain undeclared milk, a known allergen. The products were shipped to restaurant consignees in nine states.

    Product
    M.G. Waldbaum Company — Michael Foods Inc. Recalls Fair Meadow Foundations Liquid Egg Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V487000·2024-06-28

    Chevrolet Blazer EV front control arm may fracture causing control loss

    General Motors is recalling certain 2024 Chevrolet Blazer EV vehicles because the right front lower control arm may contain a manufacturing defect that can cause it to fracture.

    Product
    CHEVROLET — CHEVROLET BLAZER EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E055000·2024-06-28

    Ford Recalls Electronic Power Assist Steering Gears for Calibration Defect

    Ford is recalling 7,442 electronic power assist steering gears sold as replacement parts for 2018-2023 models due to a calibration defect that may cause the steering wheel to turn unintentionally.

    Product
    STEERING:STEERING CONTROL MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V490000·2024-06-28

    Travel trailers may have been built without a secondary emergency exit

    Forest River is recalling certain 2024-2025 Salem and Wildwood travel trailers that may not have a secondary emergency exit installed, which could prevent occupants escaping in an emergency.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V494000·2024-06-28

    Ford F-650 and F-750 tie rod ball studs can break

    Ford is recalling certain 2025 F-Super Duty F-650 and F-750 vehicles because front axle tie rod ball studs may have been incorrectly heat-treated and can break, causing tie rod failure.

    Product
    FORD — FORD F-650 SD, F-750 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V491000·2024-06-28

    Chevrolet Colorado fuel pump lock ring may leak fuel in crash

    General Motors is recalling certain 2024 Chevrolet Colorado and GMC Canyon vehicles because the lock ring securing the fuel pump may not have been fully locked, allowing a fuel leak during a crash.

    Product
    CHEVROLET — CHEVROLET, GMC COLORADO, CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V493000·2024-06-28

    Ford Mustang steering wheel can turn against the driver's intentions

    Ford is recalling certain 2022-2023 Mustang vehicles because an improperly calibrated secondary steering torque sensor can make the steering wheel turn side to side on its own.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V489000·2024-06-28

    Coachmen Cross Trail Motorhomes Recalled for Ladder Receiver Defect

    Forest River is recalling 2024-2025 Coachmen Cross Trail motorhomes because the ladder receiver may be installed without a backer, causing the ladder to detach.

    Product
    COACHMEN — COACHMEN CROSS TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V488000·2024-06-28

    Coachmen Cross Trail Motorhomes Recalled for Ladder Defect

    Forest River is recalling 2024-2025 Coachmen Cross Trail motorhomes because a missing ladder backer may cause the ladder to detach, increasing injury risk.

    Product
    COACHMEN — COACHMEN CROSS TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V495000·2024-06-28

    Lucid Air coolant heater may fail to defrost the windshield

    Lucid is recalling certain 2022-2024 Air vehicles because the high voltage coolant heater may fail to defrost the windshield, reducing the driver's view.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V496000·2024-06-28

    Ford Mustang brake warning light can stay lit masking low fluid

    Ford is recalling certain 2024 Mustang vehicles because the brake fluid level sensor may be misconfigured after a module update, leaving the warning light constantly illuminated.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V492000·2024-06-28

    Horse trailers built without a secondary gate latch can swing open

    Delco Trailers is recalling all 2019-2024 Bumper Horse trailers because they were manufactured without a secondary latch on the inside gate, which can leave the gate unlatched.

    Product
    DELCO TRAILERS — DELCO TRAILERS BUMPER HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24744·2024-06-27

    Dania Furniture Recalls Hayden Bookcase Due to Tip-Over Hazard

    Dania Furniture is recalling about 940 Hayden Bookcases sold from November 2017 through February 2024 because the bookcase can tip over and cause entrapment injuries if not anchored to the wall. A 4-year-old child died from a tip-over incident in August 2023.

    Product
    Hayden Bookcase
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24285·2024-06-27

    Brookstone TurboVac Handheld Rechargeable Vacuums Recalled for Fire Hazard

    Southern Telecom is recalling about 10,600 Brookstone TurboVac handheld rechargeable vacuums (Model BSBVAC301) due to a fire hazard caused by battery short circuits during or after charging. The firm has received two reports of serious fires resulting in property damage.

    Product
    Brookstone TurboVac Handheld Rechargeable Vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24287·2024-06-27

    Baseus Magnetic Wireless Charging Power Banks Recalled for Fire Hazard

    Shenzhen Baseus Technology is recalling about 132,000 Baseus Magnetic Wireless Charging Power Banks because the lithium-ion batteries can overheat, posing a fire hazard. The company has received 171 incident reports including 39 fires, 13 burn injuries, and about $20,000 in property damage.

    Product
    Baseus Magnetic Wireless Charging Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V483000·2024-06-27

    Altec Recalls 2021-2024 JEMS Vehicles Due to Fire Risk

    Altec is recalling 2021-2024 JEMS S and SE vehicles because A/C hoses may overheat near the exhaust manifold, increasing fire risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE JEMS HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V481000·2024-06-27

    Chevrolet Bolt battery diagnostic software may miss defective modules

    GM is recalling certain 2020-2022 Bolt EV and 2022 Bolt EUV vehicles previously remedied under 21V-650, because diagnostic software may have been installed incorrectly and fail to detect defective battery modules.

    Product
    CHEVROLET — CHEVROLET BOLT EUV, BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V482000·2024-06-27

    Lexus and Toyota head restraints can be removed without the release button

    Toyota is recalling certain 2024 Lexus RX and 2024-2025 NX vehicles because driver and front passenger head restraints may be removed inadvertently without pressing the lock release, failing FMVSS 202.

    Product
    LEXUS — LEXUS NX HYBRID, NX, RX HYBRID, RX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24284·2024-06-27

    At Home Recalls Tie Dye Fur Toy Trunk Storage Chests for Entrapment Risk

    At Home Procurement is recalling approximately 990 Tie Dye Fur Toy Trunk Storage Chests sold from September 2023 through February 2024 because they lack a lid support feature and ventilation holes, creating entrapment and suffocation hazards.

    Product
    Tie Dye Fur Toy Trunk Storage Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V480000·2024-06-27

    Volkswagen rearview camera image may be delayed or deactivated in reverse

    Volkswagen is recalling certain 2022-2024 Golf R and Golf GTI, and 2024 Atlas and Atlas Cross Sport vehicles because the rearview camera image may be delayed or deactivated after shifting into reverse.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF R, GTI, ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24283·2024-06-27

    REI Co-op Cycles REV Children's Bicycles with Training Wheels Recall

    REI is recalling Co-op Cycles REV children's bicycles (12-, 16-, and 20-inch models, 2022-2024) because the training wheel assembly knob can loosen and detach, creating fall and injury hazards.

    Product
    Co-op Cycles REV 12-, 16-, or 20-inch Kid's Bicycles with training wheels (all model years 2022-2024)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24E053000·2024-06-27

    Power Stop Recalls Braided Steel Brake Hoses for Leak Risk

    Power Stop LLC is recalling certain braided steel brake hoses that may leak or be mislabeled. A leak can reduce braking performance and increase crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V484000·2024-06-27

    Micro Bird Recalls School Buses Due to Rear Emergency Door Handle Defect

    Micro Bird is recalling 22,582 school buses because the rear emergency door handle may break, potentially delaying emergency access.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS, G5 SCHOOL BUS, T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V485000·2024-06-27

    Micro Bird Transit Bus Recall for Rear Emergency Door Handle Defect

    Micro Bird is recalling 794 transit buses because the rear emergency door handle may break, potentially delaying emergency access.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES TRANSIT BUS, G5 TRANSIT BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24286·2024-06-27

    Daikin, Amana, and Goodman Heat Pumps Recalled for Excessive Heat Risk

    Daikin Comfort Technologies is recalling about 56,000 Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps due to a power interruption defect that can cause the units to provide heat even when the thermostat is set to cooling mode, posing a risk of excessive heat exposure.

    Product
    Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1388-2024·2024-06-26

    New Seasons Market Strawberry Rhubarb Bakewell Tart Recalled for Undeclared Almond

    New Seasons Market is recalling its Strawberry Rhubarb Bakewell Tart due to undeclared almond. The 261 units distributed in Oregon and Washington pose an allergen risk to consumers with almond allergies.

    Product
    New Seasons Market Strawberry Rhubarb Bakewell Tart, packaged in a plastic clamshell with scale label. Contains Milk, Wheat, Eggs.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1374-2024·2024-06-26

    Raw Cheddar Cheese Recalled for Potential E. coli O157:H7 Contamination

    Raw Farm LLC has recalled Raw Cheddar Cheese made from unpasteurized milk due to potential E. coli O157:H7 contamination. The affected cheese was distributed to retailers in Texas, California, Colorado, and Arizona.

    Product
    Raw Cheddar Cheese, made from unpasteurized milk, 8 oz (1/2 lb), shredded, in a plastic bag, Keep Refrigerated under 40 degrees
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1372-2024·2024-06-26

    Raw Cheddar Cheese Recalled for Potential E. coli O157:H7 Contamination

    Raw Farm LLC recalls Raw Cheddar Cheese made from unpasteurized milk due to potential E. coli O157:H7 contamination. The product is distributed in TX, CA, CO, and AZ.

    Product
    Raw Cheddar Cheese, made from unpasteurized milk, 16 oz (1 lb) block, Keep Refrigerated under 40 degrees
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1373-2024·2024-06-26

    Raw Cheddar Cheese Recalled for Potential E. coli O157:H7 Contamination

    Raw Farm LLC is recalling 8 oz blocks of Raw Cheddar Cheese made from unpasteurized milk due to potential contamination with E. coli O157:H7. The affected products are distributed in Texas, California, Colorado, and Arizona.

    Product
    Raw Cheddar Cheese, made from unpasteurized milk, 8 oz (1/2 lb) block, Keep Refrigerated under 40 degrees
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1371-2024·2024-06-26

    Whole Cucumbers Recalled Due to Potential Salmonella Contamination

    Fresh Start Produce Sales, Inc. is recalling approximately 6,167 cases of whole cucumbers distributed in Florida, New Jersey, Pennsylvania, and North Carolina due to potential Salmonella contamination.

    Product
    Whole Cucumber, bulk cardboard boxes, 1 1/9 Bu, 60-72 ct cucumbers per box, 24ct box, Carton 36 ct box. Packaged in cardboard container box, color brown with Green and Red inked Accent colors. Grown and Packed by Bedner Growers, INC & Distributed by Fresh Start Produce Sales,
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2020-2024·2024-06-26

    Ventilator HAMILTON-C6 may fail to restart, risking oxygen deprivation

    Hamilton Medical AG is recalling the HAMILTON-C6 ventilator due to a sensor failure that may prevent re-initiation after reconnection, potentially causing hypoxia.

    Product
    Ventilator HAMILTON-C6, PN: 160021
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2130-2024·2024-06-26

    Ventilator Operator's Guide Recalled for Missing Critical MRI Safety Information

    ZOLL is recalling operator's guides for the ZOLL 731 Ventilator because they omit critical MRI safety information. Missing distance guidance could cause the ventilator to malfunction during MRI procedures.

    Product
    ZOLL 731 Ventilator (EMV+, AEV, Eagle II) - for MRI Compatible Devices - Operator's Guide and Quick Reference Guide (QRGs) as follows: Part Numbers: 1. 799-EGL2-02 2. 799-EGL2-02-01 3. 799-EGL2-02-04 4. 799-EGL2-02-05 5. 799-EGL2-02-08 6. 799-EGL2-02-10 7. 799-EGL2-02-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1379-2024·2024-06-26

    Snow White Chocolate Bulk Product Recalled for Potential Salmonella

    Clasen Quality Chocolate Inc. is recalling Snow White Chocolate bulk tanker product due to potential Salmonella contamination. The product was distributed across multiple states.

    Product
    Snow White Chocolate, Item #: 60949. Bulk tanker.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1383-2024·2024-06-26

    Milk Chocolate Coating Recalled for Potential Salmonella Contamination

    Clasen Quality Chocolate Inc. is recalling Milk Chocolate Flavored IC Coating distributed in nine states due to potential Salmonella contamination. The product is sold in bulk tanker format for use in food manufacturing.

    Product
    1057556 Milk Chocolate Flavored IC Coating, Item # 56546. Bulk tanker.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1377-2024·2024-06-26

    Heinen's Tuscan Salad Bowl recalled for undeclared pecan allergen

    Heinen's Tuscan Salad Bowl is recalled due to the presence of undeclared pecans, a known allergen not listed on the label. Consumers with pecan allergies face a risk of allergic reaction.

    Product
    Heinen's Tuscan Salad Bowl Ingredients: Garbanzo Beans***Disodium EDTA***Arugula, Roasted Corn***Red Bell Pepper, Dried Cranberries***Walnuts***Parmesan Cheese*** Contains: WALNUT, MILK
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1376-2024·2024-06-26

    Moore Family Farms Cheddar Cheese Curds recalled for E. coli contamination

    Moore Family Farms and Creamery Cheddar Cheese Curds are being recalled due to high coliform and E. coli levels. The recalled product was distributed in Iowa.

    Product
    Moore Family Farms and Creamery Cheddar Cheese Curds, 1 pound plastic bags, packaged with white ties
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1380-2024·2024-06-26

    Milk Chocolate Flavored Confectionery Coating Recalled for Potential Salmonella

    Clasen Quality Chocolate Inc. is recalling Milk Chocolate Flavored Confectionery Coating (Item #58710) due to potential Salmonella contamination. The bulk tanker product was distributed across nine states.

    Product
    Milk Chocolate Flavored Confectionery Coating (MB), Item #: 58710. Bulk tanker.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1381-2024·2024-06-26

    White Chocolate Wafer Recalled for Potential Salmonella Contamination

    Clasen Quality Chocolate Inc. is recalling 74,050 pounds of White Chocolate Wafer due to potential Salmonella contamination. The product was distributed to food service and ingredient suppliers across nine states.

    Product
    White Chocolate Wafer, Item # 59152. Net Wt. 50 lbs (22.68kg). Clasen Quality Chocolate 5126 West Terrace Drive, Madison, WI 53718
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1382-2024·2024-06-26

    Clasen Quality Chocolate White Confectionery Wafers Recalled for Salmonella

    Clasen Quality Chocolate is recalling NGMO White Confectionery Wafer due to potential Salmonella contamination. The product was distributed across nine states.

    Product
    NGMO White Confectionery Wafer, Item # 60975. Net Wt. 25 lbs (11.34kg). Clasen Quality Chocolate 5126 West Terrace Drive, Madison, WI 53718
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1378-2024·2024-06-26

    Milk Chocolate Confectionery Drops Recalled for Potential Salmonella Contamination

    Clasen Quality Chocolate is recalling 18,800 lbs of milk chocolate confectionery drops due to potential Salmonella contamination. The product was distributed across nine states.

    Product
    1085343 10M Milk Chocolate Flavored Confectionery Drop (MB), Item #: 56074. Net Wt. 25lbs (11.34kg). Distributed by: Clasen Quality Chocolate 5126 West Terrace Drive, Madison, WI 53718. Chocolate Coating products.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1385-2024·2024-06-26

    Milk Chocolate Confectionery Coating Recalled for Potential Salmonella

    Clasen Quality Chocolate Inc. is recalling Milk Chocolate Flavored Confectionery Coating Bulk (Item #60692) due to potential Salmonella contamination. The product was distributed across nine U.S. states.

    Product
    Milk Chocolate Flavored Confectionery Coating Bulk (MB), Item # 60692.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2145-2024·2024-06-26

    FDA Recalls VICRYL Plus Antibacterial Sutures Due to Packaging Defect

    Ethicon is recalling VICRYL Plus Antibacterial Sutures due to a packaging machine defect that created holes in the primary packaging, potentially compromising product sterility. Affected sutures may pose an infection risk.

    Product
    VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, except for ophthalmic, cardiovascular and neurological tissues. PRODUCT CODE: VCP196H VCP417H VCP602H VCP603H VCP662H VCPB259H VCPB94
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2146-2024·2024-06-26

    PDS II Polydioxanone Sutures Recalled Due to Compromised Sterility

    Ethicon is recalling 56,952 units of PDS II polydioxanone sutures distributed worldwide because a packaging defect resulted in compromised sterility, which could lead to infection. No illnesses have been reported.

    Product
    PDS II (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric cardiovascular tissue, in microsurgery and in ophthalmic surgery. These sutures are particularly useful where the combination of an absorbable suture and extended wo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0560-2024·2024-06-26

    White Petrolatum Jelly Mislabeled With Undisclosed Lavender and Chamomile

    Consumer Product Partners is recalling Pure Petroleum white petrolatum products sold at Rite Aid, Kroger, Harris Teeter, and CVS nationwide because the products labeled as pure white petrolatum actually contain undisclosed lavender and chamomile.

    Product
    PURE PETROLEUM — PURE PETROLEUM (WHITE PETROLATUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2161-2024·2024-06-26

    Xstar Safety Slit Knife Recalled for Incorrect Blade Bevel Orientation

    Beaver Visitec International is recalling the Xstar Safety Slit Knife Model 378227 because some units have the blade bevel installed incorrectly—facing downward instead of the intended upward orientation.

    Product
    Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0559-2024·2024-06-26

    Cefixime Oral Suspension Recalled for Failed Content Uniformity Specifications

    Lupin Pharmaceuticals is recalling one lot of Cefixime oral suspension (200 mg/5 mL) due to failed content uniformity specifications. The recall affects 3,552 bottles distributed nationwide.

    Product
    CEFIXIME — CEFIXIME (CEFIXIME)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2144-2024·2024-06-26

    VICRYL Sutures recalled due to packaging defect compromising sterility

    Ethicon recalls 341,532 units of VICRYL surgical sutures worldwide due to holes in primary packaging that compromise sterility and could result in infection.

    Product
    VICRYL (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic surgery, but not for use in cardiovascular and neurological tissues. PRODUCT CODE: J214H J218H J258H J268H J269H J327H J344H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2149-2024·2024-06-26

    Ethicon MONOCRYL Plus Sutures Recalled for Packaging Defect

    Ethicon recalled 287,892 MONOCRYL Plus Antibacterial Sutures worldwide due to a packaging machine defect that created holes in primary packaging, potentially compromising sterility and risking infection.

    Product
    MONOCRYL Plus Antibacterial (poliglecaprone 25) Suture - Intended for use in general soft tissue approximation and/or ligation where an absorbable material is indicated. PRODUCT CODE: MCP266H13 MCP3200H16 MCP3212H16 MCP3213H16 MCP340H13 MCP345H13 MCP416H14 MCP417H14 M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2154-2024·2024-06-26

    Bard Foley Catheter Trays Recalled for Temperature Display Malfunction

    C.R. Bard Inc is recalling 6,420 Foley catheter trays nationwide because some devices may not display temperature readings or may display erratic readings. The malfunction could affect patient monitoring.

    Product
    Bard Medical SureStep Foley Tray System, 16 Fr., Catalog #A319416AM; and Bard Medical Bardex IC Complete Care Infection Control Temperature-Sensing Foley Catheter Tray with Bard Hydrogel and Bacti-Guard Silver Alloy Coating, 350 ml Urine Meter, 16 Fr, Catalog #319416AM. Intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V478000·2024-06-26

    Thomas Built Buses Recall School Buses for Emergency Alarm Defect

    Daimler Trucks North America is recalling 162 Thomas Built Buses Saf-T-Liner C2 and C2 Jouley school buses because the emergency exit alarm may not sound.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2, SAF-T-LINER C2 JOULEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2150-2024·2024-06-26

    TabloCart power cord connector may overheat in hemodialysis system

    Outset Medical is recalling 431 TabloCart hemodialysis system carts due to power cord connector defects that may cause overheating, sparks, and smoke, potentially delaying treatment or causing burns.

    Product
    TabloCart with Prefiltration Drawer PN-0006813, with power cords: PN-0005746 (10-foot), PN-0006578 (15-foot), PN-0005747 (20-foot)10-, 15- and 20-foot cords respectively), used with the Tablo Hemodialysis System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0558-2024·2024-06-26

    OSSOS-SANS tablets recalled: undeclared diclofenac and methocarbamol found

    OSSOS-SANS Reforzado tablets are being recalled because they contain undeclared active pharmaceutical ingredients—diclofenac and methocarbamol—and were marketed without FDA approval.

    Product
    OSSOS-SANS Reforzado con: Glucosamina Curcuma Ortiga tablets, packaged in a 30-count bottle, DISTRIBUIDOR POR: Naturistas Especializados, Alce Blanco 180-A Fracc. Industrial, Edo. de Mexico C.P. 53370
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1387-2024·2024-06-26

    Caramel Confectionery Drops Recalled for Potential Salmonella Contamination

    Clasen Quality Chocolate Inc. is recalling 4M Caramel Flavored Confectionery Drop due to potential Salmonella contamination. The product was distributed to nine states.

    Product
    4M Caramel Flavored Confectionery Drop, Item # 61661 (R&D Sample).
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1386-2024·2024-06-26

    Milk Chocolate Wafer recalled for potential Salmonella contamination

    Clasen Quality Chocolate Inc. is recalling Milk Chocolate Wafer (Item #51407) distributed in nine states due to potential Salmonella contamination.

    Product
    Milk Chocolate Wafer, Item # 51407 (R&D Sample).
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2162-2024·2024-06-26

    Xstar Safety Slit Knife Recalled for Incorrect Blade Configuration

    Beaver Visitec International is recalling 126 Xstar Safety Slit Knives with incorrect blade configuration. The recalled knives have the bevel oriented to the back instead of the front.

    Product
    Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227, a component of CustomEye Kits, Numbers 584562, 5800109
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2152-2024·2024-06-26

    Storage Case Design Flaw May Allow Reuse of Single-Use Surgical Instruments

    Howmedica Osteonics Corp. is recalling HRIS Storage & Sterilization Cases (Part 6210-9-900) due to a design flaw that may allow reuse and resterilization of single-use, sterile instruments. This poses a contamination and infection risk.

    Product
    HRIS Storage & Sterilization Case and Tray, Catalog/Part Number: 6210-9-900
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0555-2024·2024-06-26

    FDA Recalls Dexamethasone Sodium Phosphate Injection Due to Impurity Specification Failure

    Eugia US LLC recalls 70,125 vials of Dexamethasone Sodium Phosphate injection due to failed impurity specifications. Testing found sulfonic acid adduct of dexamethasone phosphate exceeded allowed limits.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2147-2024·2024-06-26

    PDS Plus Antibacterial Surgical Sutures Recalled for Compromised Sterility

    Ethicon recalls PDS Plus Antibacterial sutures due to packaging defects that compromised sterility. The affected units may cause infection if used in surgery.

    Product
    PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric cardiovascular tissue, in microsurgery and in ophthalmic surgery. These sutures are particularly useful where the combination of an absorbable suture
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2153-2024·2024-06-26

    Howmedica Gray Revision Instrument Tray Recalled for Design Enabling Instrument Reuse

    Howmedica is recalling the Gray Revision Instrument System Accessory Tray/Case due to a design flaw that may enable reuse and re-sterilization of single-use, sterile-packaged instruments.

    Product
    Gray Revision Instrument System Accessory Tray/Case, Catalog/Part Number: 6210-9-910
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2155-2024·2024-06-26

    Exactech Knee Patella Components Recalled Due to Out-of-Specification Vacuum Bags

    Exactech is recalling OPTETRAK Three Peg Patella knee components packaged in out-of-specification vacuum bags. The affected products were distributed worldwide.

    Product
    OPTETRAK Three Peg Patella, Item Numbers: a) 200-02-26, 26MM; b) 200-02-29, 29MM; c) 200-02-32, 32MM; d) 200-02-35, 35MM; e) 200-02-38, 38MM; f) 200-02-41, 41MM;
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2157-2024·2024-06-26

    OPTETRAK Inset Patella knee implants recalled for improper vacuum packaging

    Exactech is recalling OPTETRAK Inset Patella knee implants packaged in out-of-specification vacuum bags that may compromise product integrity during storage or sterilization.

    Product
    OPTETRAK Inset Patella, Item Numbers: a) 200-05-23, 23MM; b) 200-05-26, 26MM; c) 200-05-29, 29MM
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2148-2024·2024-06-26

    MONOCRYL Surgical Sutures Recalled for Packaging Sterility Defect

    Ethicon recalls 306,000 MONOCRYL surgical sutures worldwide due to holes in primary packaging from a manufacturing defect that compromises sterility and could result in infection.

    Product
    MONOCRYL (poliglecaprone 25) Suture - Intended for use in general soft tissue approximation and/or ligation where an absorbable material is indicated PRODUCT CODE: Y315H Y345H Y359H Y398H Y416H Y417H Y426H Y427H Y935H Y936H Y945H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2151-2024·2024-06-26

    Hospital bed mattress covers may delaminate from improper cleaning

    Baxter Healthcare is recalling Centrella Max and Pro+ hospital bed mattresses that may develop delaminated top covers when cleaned with bleach-containing solutions. The mattresses prevent and treat pressure injuries.

    Product
    Centrella Max - The Centrella Smart+ Bed is intended for use in healthcare environments as a patient support system to prevent and/or treat pressure injuries.Multiple model numbers of Centrella Max mattresses and pro+ mattresses. (1) Centrella Max Surface, REF P7922A01; (2) C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0561-2024·2024-06-26

    Teva Recalls Amoxicillin-Clavulanate Antibiotic Tablets Due to Subpotency

    Teva Pharmaceuticals is recalling 34,448 bottles of Amoxicillin and Clavulanate Potassium Tablets USP (Chewable 400mg/57mg) distributed nationwide due to subpotency. The recall is voluntary and initiated by the firm.

    Product
    Amoxicillin and Clavulanate Potassium Tablets USP, Chewable 400mg/57mg, 20-count bottles, Rx only, Manufactured in Canada By: Teva Canada Limited, Toronto, Canada M1B 2K9; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0093-2272-34
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0557-2024·2024-06-26

    Little Remedies Gas Relief Drops Class II Recall for Manufacturing Deviations

    Denison Pharmaceuticals recalls 113,544 bottles of Little Remedies Gas Relief Drops (Lot #0855, exp. 8/31/2025) due to manufacturing deviations. All units have been recovered and controlled at the manufacturer.

    Product
    LITTLE REMEDIES — LITTLE REMEDIES (SIMTHICONE)
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Drugs)·D-0562-2024·2024-06-26

    Prescription Drug Duloxetine Recalled for Nitrosamine Impurity Exceeding FDA Limits

    Breckenridge Pharmaceutical recalls Duloxetine 60mg capsules nationwide due to N-nitroso-duloxetine impurity levels exceeding FDA interim limits. Affected lots had current good manufacturing practice (CGMP) deviations.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2160-2024·2024-06-26

    NxStage PureFlow-B Hemodialysis Solution Bags Recalled Due to Bursting Chambers and Caustic Fluid

    NxStage PureFlow-B hemodialysis solution bags may burst during preparation, releasing caustic electrolyte fluid that can cause chemical burns. Affected units are distributed nationwide.

    Product
    NxStage PureFlow-B Solution, Premixed Dialysate for Hemodialysis, Device Catalog Numbers RFP-400, RFP-401, RFP-402, RFP-403, RFP-404, RFP-405, RFP-406, RFP-453, RFP-454, RFP-456
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2158-2024·2024-06-26

    Exactech OPTETRAK Knee Implants Recalled for Out-of-Specification Vacuum Bag Packaging

    Exactech is recalling OPTETRAK Advanced Patella knee implant components packaged in vacuum bags that did not meet manufacturing specifications. Improper packaging could compromise product sterility.

    Product
    OPTETRAK, Advanced Patella, 3 Peg Implant, Item Numbers: a) 200-07-26, 26MM; b) 200-07-29, 29MM; c) 200-07-32, 32MM; d) 200-07-35, 35MM; e) 200-07-38, 38MM
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2156-2024·2024-06-26

    OPTETRAK One Peg Patella components recalled for out-of-specification vacuum bags

    Exactech is recalling OPTETRAK One Peg Patella knee implants due to vacuum bags packaged below specification. The recall affects units with multiple lot numbers distributed worldwide.

    Product
    OPTETRAK One Peg Patella,, Item Numbers: a) 200-03-26, 26MM; b) 200-03-29, 29MM; c) 200-03-32, 32MM; d) 200-03-35, 35MM; e) 200-03-38, 38MM; f) 200-03-41, 41MM
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0556-2024·2024-06-26

    Drug Recall: Eptifibatide Injection Due to Failed Degradation Specifications

    Eugia US LLC is recalling 15,500 vials of Eptifibatide injection nationwide due to failed impurities and degradation specifications. The defect involves a related substance identified as Eptifibatide dimer.

    Product
    EPTIFIBATIDE — EPTIFIBATIDE (EPTIFIBATIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V475000·2024-06-25

    SEA Electric Recalls 174 Vehicles Due to Battery Software Defect

    SEA Electric is recalling 174 vehicles because a software defect may cause the high-voltage battery to shut down, resulting in a loss of drive power.

    Product
    SEA ELECTRIC — SEA ELECTRIC FORD F59, 5E, ISUZU NRR, HINO 195
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24281·2024-06-25

    MGA Entertainment Recalls Miniverse Make It Mini Sets with Liquid Resins

    MGA Entertainment recalls about 21 million Miniverse Make It Mini Sets with unused liquid resins due to risk of skin, eye, and respiratory irritation. The recalled sets contain acrylates in amounts prohibited in children's products.

    Product
    Miniverse Make It Mini Sets with Liquid Resins
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24E052000·2024-06-25

    SEA Electric Recalls Electric Vehicle Battery Management Software

    SEA Electric is recalling certain electric vehicles because a software defect in the battery management system can cause a loss of drive power, increasing crash risk.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY:MANAGEMENT SYSTEM/ENERGY CONTROL MODULE (BMS/BECM):SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V471000·2024-06-24

    Oshkosh Defense NGDV ICE Recalled for Air Bag Deployment Risk

    Oshkosh is recalling 2025 Defense NGDV ICE vehicles because deformed wiring harness terminals may prevent air bags from deploying as intended.

    Product
    OSHKOSH — OSHKOSH DEFENSE NGDV ICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V451000·2024-06-24

    Jaguar F-Pace oil filter housings can crack and leak oil

    Jaguar is recalling certain 2021-2024 F-Pace vehicles because the oil filter housing can crack and leak oil into the engine compartment. 150 units are affected.

    Product
    JAGUAR — JAGUAR F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V467000·2024-06-21

    Isuzu Recalls 2025 FTR Trucks Due to Tie Rod Assembly Defect

    Isuzu is recalling 2025 FTR vehicles because incorrectly heat-treated ball studs in the tie rod assemblies may break, potentially causing loss of steering control.

    Product
    ISUZU — ISUZU FTR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V468000·2024-06-21

    REV Ambulance Recalls 2019-2024 Vehicles Due to Outrigger Bolt Defect

    REV Ambulance is recalling 160 emergency vehicles because improperly tightened outrigger bolts may cause the module box to detach or the outrigger to fail.

    Product
    REV AMBULANCE — REV AMBULANCE TYPE IX, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E050000·2024-06-21

    AROW Recalls MV210 Emergency Exit Windows Due to Latch Failure Risk

    AROW Global Corp is recalling MV210 emergency exit windows because the latch can fail during a crash, potentially allowing the window to open and increasing injury risk.

    Product
    STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT:LATCHING/RELEASE SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24271·2024-06-20

    myCharge POWER HUB Portable Chargers Recalled for Fire and Burn Hazards

    myCharge is recalling about 567,000 POWER HUB All-In-One 10,000mAh portable chargers sold exclusively at Costco from January 2022 through November 2023 because they can overheat while charging, posing fire and burn hazards. Two residential fires and property damage totaling approximately $165,000 have been reported.

    Product
    myCharge POWER HUB All-In-One 10,000mAh portable chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V465000·2024-06-20

    Audi e-tron GT front axle brake hoses may tear and leak

    Volkswagen is recalling certain 2022-2024 Audi RS e-tron GT and e-tron GT vehicles because the front axle brake hoses can develop tears, causing a leak and brake circuit failure.

    Product
    AUDI — AUDI E-TRON GT, RS E-TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V463000·2024-06-20

    Navistar Recalls 2025 IC Bus CE School Buses for Tie Rod Defect

    Navistar is recalling 2025 IC Bus CE school buses because incorrectly heat-treated tie rod assemblies may break, potentially causing loss of steering control.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V462000·2024-06-20

    International truck tie rod ball studs were incorrectly heat treated

    Navistar is recalling certain 2025 International HV, LT, MV and RH trucks because tie rod ball studs may have been incorrectly heat-treated and can break. 116 units affected.

    Product
    INTERNATIONAL — INTERNATIONAL RH, HV, MV, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24272·2024-06-20

    JoyJolt Declan Glass Coffee Mugs Recalled for Burn and Laceration Hazards

    MM Products is recalling about 580,000 JoyJolt Declan single-wall glass coffee mugs because they can break and crack when filled with hot liquids, posing burn and laceration hazards. The mugs were sold online from September 2019 through May 2022.

    Product
    JoyJolt Drinkware Declan Single-Wall Glass Coffee Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E051000·2024-06-20

    Hendrickson Lift Axle Suspension Recall for Tie Rod Assembly Defect

    Hendrickson is recalling 461 steerable lift axle suspension assemblies because the tie rod ball stud may fail, creating a road hazard.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24273·2024-06-20

    Frontgate Newport Chaise Lounge Chairs Recalled for Finger Crushing and Amputation

    Cinmar recalls approximately 70,000 Frontgate Resort Collection Newport aluminum and teak chaise lounge chairs because the adjustable backrest can descend with force while seated, causing finger crushing and amputation injuries.

    Product
    Frontgate Resort Collection Newport Aluminum and Teak Chaises
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V461000·2024-06-20

    Toyota Grand Highlander curtain airbags may deploy outside an open window

    Toyota is recalling certain 2024 Grand Highlander and Lexus TX vehicles because the side curtain airbags may not unroll as intended and could partially deploy outside an open window.

    Product
    TOYOTA — TOYOTA, LEXUS GRAND HIGHLANDER, TX, GRAND HIGHLANDER HYBRID, TX HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V459000·2024-06-20

    Cadillac XT5 and XT6 instrument panels may not illuminate signal reminders

    GM is recalling certain 2023-2025 Cadillac XT5 and XT6 vehicles because the instrument panel may not illuminate when hazard warning lights, high beams or turn signals are activated.

    Product
    CADILLAC — CADILLAC XT5, XT6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V464000·2024-06-20

    Volkswagen Atlas occupant detection wiring may deactivate the passenger airbag

    Volkswagen is recalling certain 2020-2024 Atlas and Atlas Cross Sport vehicles because a wiring fault in the passenger occupant detection system may deactivate the front passenger airbag.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V466000·2024-06-20

    Fisker Ocean exterior door handles can stick and fail to open

    Fisker is recalling all 2023-2024 Ocean vehicles because the exterior door handles can stick and fail to open, which can prevent occupants from exiting in an emergency.

    Product
    FISKER — FISKER OCEAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24276·2024-06-20

    Vitamix Blending Containers and Blade Bases Recalled for Laceration Hazard

    Vitamix Ascent and Venturist Series 8-ounce and 20-ounce blending containers and blade bases can separate from their bases, exposing sharp blades. The company has received 27 reports of lacerations, including 11 from a previous 2018 recall.

    Product
    Vitamix Ascent® Series and Venturist® Series 8-ounce and 20-ounce Blending Containers and Blade Bases
    Category
    Consumer Product
    Distribution
    Distributed nationwide

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