The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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22226–22250 of 39678

  • SevereFDA (Food)·F-0723-2017·2016-12-21

    Request Foods Recalls Cheese Manicotti for Undeclared Eggs

    Request Foods Inc. is recalling GFS Cheese Manicotti in tomato sauce due to undeclared eggs. The product was distributed in Michigan, Ohio, Florida, and Kentucky.

    Product
    GFS Cheese Manicotti in tomato sauce. retail 68 oz. pan. 4 retail units per case
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0185-2017·2016-12-21

    Cantrell Drug Company Recalls Phenylephrine HCl Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 30,796 syringes of Phenylephrine HCl 1 mg/10 mL due to a lack of assurance of sterility. The recall covers products distributed nationwide.

    Product
    Phenylephrine HCl 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 mL Single-Dose Syringe, Rx Only Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-171-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0200-2017·2016-12-21

    Cantrell Drug Recalls Neostigmine Methylsulfate Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling specific lots of Neostigmine Methylsulfate injection syringes because the firm cannot ensure the products are sterile.

    Product
    Neostigmine Methylsulfate 5 mg/5 mL Injection Solution, 5 mL (1 mg/mL) Single-Dose Syringe, For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-046-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0201-2017·2016-12-21

    Cantrell Drug Company Recalls Oxytocin Injection Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 2,681 bags of Oxytocin 30 USP Units due to a lack of assurance of sterility. The affected product is distributed nationwide.

    Product
    Oxytocin 30 USP Units Added to 0.9% Sodium Chloride, 500 mL Bag, Single-Dose Bag, Injection Solution for IV Use Only, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-056-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0693-2017·2016-12-21

    Mary's Homemade Vegetable Soup Recalled for Botulism Risk

    Mary's Homemade Vegetable Soup is being recalled because it is underprocessed and may pose a Clostridium Botulinum hazard.

    Product
    Mary's Home Made Vegetable Soup; 16 FL. OZ. (1 Pint) OR 32 FL. OZ. (1 Quart); Heat and Serve
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0197-2017·2016-12-21

    Cantrell Drug Recalls Lidocaine HCl Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 162 syringes of Lidocaine HCl 1% because the firm cannot assure the sterility of the product.

    Product
    Lidocaine HCl 1%, 10 mL Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0692-2017·2016-12-21

    Green Cuisine Recalls Pesto Pasta Salad Due to Listeria Risk

    Green Cuisine, Inc. is recalling Pesto Pasta Salad with Arugula because it may be contaminated with Listeria monocytogenes.

    Product
    Pesto Pasta Salad with Arugula, Net Wt. 16oz, UPC 857898004333
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0707-2017·2016-12-21

    Troyer Cheese Recalls Peanut Butter Pretzels for Listeria Risk

    Troyer Cheese Inc is recalling Backroad Country Peanut Butter Pretzels due to potential Listeria monocytogenes contamination. The product was distributed to 26 states.

    Product
    BACKROAD COUNTRY PEANUT BUTTER PRETZELS, Net Wt. 7 oz (198g) Product Code 15372 BEST IF USED BY 05/2017
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0700-2017·2016-12-21

    First Source Recalls Oriental Snack Mix for Listeria Risk

    First Source LLC is recalling specific lots of Oriental Snack Mix due to potential Listeria monocytogenes contamination. The product was distributed to retail stores in 11 states.

    Product
    Oriental Snack Mix under the following labels: 1) Flave! ORIENTAL MIX, NET WT 6OZ (170g), shipped 12 packs per case, 2) Alpine Valley Oriental Snack Mix, 4oz 3) 15 LB Bulk ALPINE VALLEY ORIENTAL DELIGHT MIX, shipped 1 per case
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-0196-2017·2016-12-21

    Cantrell Drug Recalls Hydromorphone Injection Vials Due to Sterility Concerns

    Cantrell Drug Company is recalling 93 vials of Hydromorphone HCl injection solution nationwide due to a lack of assurance of sterility.

    Product
    Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride 30 mL PCA Vial (1 mg/mL), Single-Dose Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0109-2017·2016-12-21

    Apple Tree Goat Dairy Chevre Recalled for Listeria Contamination

    Apple Tree Goat Dairy is recalling all lots of its 8 oz and 5 lb Chevre products due to potential Listeria monocytogenes contamination.

    Product
    Apple Tree Goat Dairy Chevre, Net Wt. 8 oz. shrink wrap and wt. 5 lb blocks, Richfield, PA 17086.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0694-2017·2016-12-21

    First Source LLC Recalls Fitness Mix for Listeria Contamination Risk

    First Source LLC is recalling multiple varieties of Fitness Mix due to the potential for Listeria monocytogenes contamination. The product was distributed to retail stores in 11 states.

    Product
    FITNESS MIX sold under the following labels: 1) 15 LBS ALPINE VALLEY FITNESS MIX, packed as 1 per case, 2) Wegmans square tub FITNESS MIX, 20 oz, packed as 12 per case, Flave! FITNESS MIX, NET WT 8OZ (226g), packed as 12 per case, 4) FITNESS MIX, NET WT 5 OZ (141g), shipped 6…
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0733-2017·2016-12-21

    Publix Danish Maple Walnut Coffee Cake Recalled for Metal Shavings

    Publix Super Markets is recalling Danish Maple Walnut Coffee Cake strips due to the presence of small metal shavings.

    Product
    Publix Danish Maple Walnut Coffee Cake Strip, 14 oz. UPC 002-19562-00000
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0186-2017·2016-12-21

    Cantrell Drug Company Recalls Calcium Chloride Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 73 bags of Calcium Chloride in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag, Rx Only, Single-Dose Bag Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-102-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0204-2017·2016-12-21

    Cantrell Recalls Succinylcholine Chloride Injection Due to Sterility Concerns

    Cantrell Drug Company is recalling specific lots of Succinylcholine Chloride 200 mg/10 mL injection syringes because the firm cannot ensure the products are sterile.

    Product
    Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL (20 mg/mL) ,Single-Dose Syringe Injection Solution, For Slow IV Use Only ,Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-067-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0685-2017·2016-12-21

    Topnotch Foods Bread Crumbs Recalled for Undeclared Allergens

    Topnotch Foods is recalling Regular Bread Crumbs in bulk bags because they contain undeclared egg, tree nuts, and milk.

    Product
    Topnotch Foods Regular Bread Crumbs 2,000 lb. bulk bag, 50 lb. bulk bag, and 10 lb. bulk bag
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0203-2017·2016-12-21

    Cantrell Drug Recalls Ropivacaine HCl Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 87 bags of Ropivacaine HCl 0.25% due to a lack of assurance of sterility. The product is intended for epidural use only.

    Product
    Ropivacaine HCl 0.25% in 0.9% Sodium Chloride, 100 mL Bag, Epidural Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-185-75
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V913000·2016-12-20

    Volkswagen Recalls 2009-2010 Models for ABS Control Unit Failure

    Volkswagen is recalling 2009-2010 Jetta, GTI, Golf, and Audi A3 vehicles because the ABS control unit may fail, potentially causing loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI JETTA SPORTWAGEN, JETTA, GTI, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17056·2016-12-20

    Zebra Thermal Printer Power Supply Units Recalled for Fire Hazard

    Zebra Technologies is recalling approximately 166,000 power supply units for thermal printers due to a fire hazard caused by overheating and corrosion.

    Product
    Power supply units for Zebra brand thermal printers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16C008000·2016-12-19

    Baby Trend Recalls Booster Seats Due to Harness Rivet Failure Risk

    Baby Trend is recalling specific Hybrid LX booster seats because a center adjuster rivet may break if used with children over 40 lbs, increasing injury risk in a crash.

    Product
    CHILD SEAT:HARNESS:STRAP/WEBBING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17055·2016-12-16

    LG Recalls Portable Air Conditioners Due to Fire Hazard

    LG Electronics is recalling about 466,000 portable air conditioners sold in the U.S. because they can overheat and cause fires.

    Product
    Portable Air Conditioners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·118-2016·2016-12-15

    R&R Provision Recalls Breaded Veal Products Due to Undeclared Allergens

    R&R Provision Company is recalling approximately 23,040 pounds of breaded veal products because they contain undeclared whey and nonfat milk.

    Product
    Schiff's Food Service, Inc., DBA R&R Provision Company — R&R Provision Company Inc. Recalls Breaded Veal Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0589-2017·2016-12-14

    Club Chef Broccoli and Raisin Salad Kits Recalled for Listeria Risk

    Club Chef LLC is recalling Broccoli & Raisin Salad Kits because the supplier reported potential Listeria monocytogenes contamination.

    Product
    Club Chef Broccoli & Raisin Salad Kits, in 7.625 lb cases, containing 1bag (4.8 oz) of Raisin Sunflower Mix per case.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0601-2017·2016-12-14

    Agave Dream Lavender Recalled for Potential Listeria Contamination

    Agave Dream is recalling 1 Pint Lavender products due to potential Listeria monocytogenes contamination. The product was distributed in eight U.S. states.

    Product
    Agave Dream Lavender 1 Pint UPC Code 8 9934900206 2
    Category
    Food
    Distribution
    8 states