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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

21776–21800 of 39678

SevereFDA (Drugs)·D-0322-2017·2017-01-11
Tri-Coast Pharmacy Recalls Ultra Amino Energy Cocktail Due to Sterility Concerns
Tri-Coast Pharmacy is recalling 870 vials of Ultra Amino Energy Cocktail nationwide due to a lack of assurance of sterility.
Product
Ultra Amino Energy Cocktail (Methionine (L) 12.5mg/Inositol 25mg/Choline Chloride 25 mg/Methylcobalamin 300mcg/Carnitine (L) 125mg/Thiamine HCL 50mg/Riboflavin-5-Phosphate Sod 5mg/Miacinamide 20mg/Pyridoxine HCL 2mg/Folic Acid 2mg/Ascorbic Acid 50mg/Chromium Picolinate…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1158-2017·2017-01-11
FDA Recalls Herring Fillets for Potential Listeria Contamination
Royal Seafood Baza, Inc. is recalling refrigerated herring fillets due to potential Listeria monocytogenes contamination. Consumers should check their freezers for affected products.
Product
Refrigerated, Ready to Eat Herring Fillets in oil Lightly Salted sold under the FRESH SEAFOOD label, packaged in a plastic retail container (tub), Net Wt. 16 oz. (454g) - UPC 825512 014044 --- Produced by Royal Seafood Baza U.S.A.
Category
Food
Distribution
7 states
SevereFDA (Drugs)·D-0406-2017·2017-01-11
Wells Pharmacy Recalls TitanMax Injectable Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling 18 vials of TitanMax-MIC/12/CA/CH/L/D Injectable due to a lack of assurance of sterility. The product was distributed nationwide.
Product
TitanMax-MIC/12/CA/CH/L/D Injectable 25 mg/50 mg/50/0.5 mg/50 mg/25 mcg/25 mg/25 mg/mL, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0362-2017·2017-01-11
Wells Pharmacy Recalls Indocyanine Green Injectable Kits Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling 131 kits of Indocyanine Green (P.F.) 15 mg Injectable due to a lack of assurance of sterility.
Product
Indocyanine Green (P.F.), 15 mg Injectable Kit, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0336-2017·2017-01-11
FDA Recalls Compounded HCG Injectable Kits Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling 10 kits of compounded Chorionic Gonadotropin (HCG) injectable kits due to a lack of assurance of sterility.
Product
Chorionic Gonadotropin, Lyophilized (HCG) 11,000 Unit Injectable Kit, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0343-2017·2017-01-11
Wells Pharmacy Recalls Bimix Injectable Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling Bimix 30 mg/1 mg/mL Injectable vials because the product lacks assurance of sterility.
Product
Bimix 30 mg/1 mg/mL Injectable, a) 5 mL and b) 10 mL vial, Compounded by Wells Pharmacy Network, LLC, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0256-2017·2017-01-11
Tri-Coast Pharmacy Recalls Dexpanthenol Due to Sterility Concerns
Tri-Coast Pharmacy is recalling Dexpanthenol 250 mg/mL vials because the agency could not ensure the products were sterile.
Product
Dexpanthenol 250 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0844-2017·2017-01-11
Country Fresh Jal Ched Stuff Mushrooms Recalled for Listeria Risk
Country Fresh Products is recalling Harris Teeter Jal Ched Stuff Mushrooms due to potential Listeria monocytogenes contamination.
Product
Harris Teeter, Jal Ched Stuff Mushrooms 7oz
Category
Food
Distribution
12 states
SevereFDA (Drugs)·D-0384-2017·2017-01-11
Wells Pharmacy Recalls QUAD2 Injectable Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling QUAD2 injectable vials because they may not be sterile. The recall covers vials prepared between February and September 2016.
Product
QUAD2 (PAP/PHEN/ALPROS/ATRO) 9 mg/1 mg/10 mg/0.1 mg/mL Injectable a) 2 mL and b) 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1153-2017·2017-01-11
Royal Seafood Baza Recalls Herring Fillets for Listeria Risk
Royal Seafood Baza is recalling refrigerated herring fillets sold as 'Matjes' due to potential Listeria monocytogenes contamination.
Product
Refrigerated, Ready to Eat Herring in Brine, Herring Fillet "Matjes" sold under the FRESH SEAFOOD label, packaged in plastic retail containers (tubs), Net Wt. 10.9 oz. (310g) - UPC 825512 004953 and Net Wt. 16.2 oz. (460g) - UPC 825512 004960 -- Manufactured by R.S.B. NY 10303
Category
Food
Distribution
7 states
SevereFDA (Drugs)·D-0358-2017·2017-01-11
Wells Pharmacy Recalls Injectable Compounds Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling 147 vials of a compounded injectable drug due to a lack of assurance of sterility. The products were distributed nationwide.
Product
Glutamine/ORNI/Arginine/LYS/CITRU+LIDO 75 mg/75 mg/150 mg/50 mg/100 mg/10 mg/mL Injectable, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0392-2017·2017-01-11
FDA Recalls Sermorelin Acetate Injectable Kits Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling Sermorelin Acetate/GHRP (2) Injectable Kits nationwide due to a lack of assurance of sterility.
Product
Sermorelin Acetate/GHRP (2) Kit 6 mg/4.5 mg Injectable Kit, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0298-2017·2017-01-11
Tri-Coast Pharmacy Recalls Testosterone Cypionate Due to Sterility Concerns
Tri-Coast Pharmacy is recalling 400 vials of compounded Testosterone Cypionate in Sesame because the products lack assurance of sterility.
Product
Testosterone Cypionate in Sesame, 150 mg/mL, (5 ML). Compounded by Tri-Coast Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0334-2017·2017-01-11
Wells Pharmacy Recalls Ultra-Test Injectable Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling 714 vials of Ultra-Test in Grapeseed Oil Injectable due to a lack of assurance of sterility. The product was distributed nationwide.
Product
ULTRA-TEST in Grapeseed Oil (CYP 90%/PROP 10%) Injectable, 200 mg/mL, 8 mL vial, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0373-2017·2017-01-11
Wells Pharmacy Recalls MIC/B-COMP+LIDO Injectable Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling MIC/B-COMP+LIDO 20 mg/40 mg/50 mg/10 mg/mL Injectable vials due to a lack of assurance of sterility.
Product
MIC/B-COMP+LIDO 20 mg/40 mg/50 mg/10 mg/mL Injectable, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0330-2017·2017-01-11
Wells Pharmacy Recalls QUAD3 Injectable Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling QUAD3 injectable vials because the FDA determined there is a lack of assurance of sterility.
Product
QUAD3 (PAP/PHEN/ALPRO/ATRO) 30 mg/3 mg/30 mcg/0.1mL Injectable, a) 2 mL and 5 mL vials, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0254-2017·2017-01-11
Tri-Coast Pharmacy Recalls Calcium Gluconate Injection Due to Sterility Concerns
Tri-Coast Pharmacy is recalling 12 vials of Calcium Gluconate 10% Injection compounded between May and November 2016 due to a lack of assurance of sterility.
Product
Calcium Gluconate 10% Injection (30 ML). Compounded by Tri-Coast Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1137-2017·2017-01-11
Chapel Hill Creamery Recalls Burrata Due to Salmonella Contamination Risk
Chapel Hill Creamery LLC is recalling retail burrata sold in water due to potential Salmonella contamination. The product was distributed in five southeastern states.
Product
Burrata, is sold by each, retail only, packaged in water.
Category
Food
Distribution
5 states
SevereFDA (Drugs)·D-0252-2017·2017-01-11
Tri-Coast Pharmacy Recalls BiMix Phentolamine/Papaverine Due to Sterility Concerns
Tri-Coast Pharmacy is recalling BiMix Phentolamine/Papaverine vials because the agency could not ensure the products were sterile.
Product
BiMix Phentolamine/Papaverine 1 mg/30 mg/mL (1 ML). Compounded by Tri-Coast Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0370-2017·2017-01-11
Wells Pharmacy Recalls Injectable Compounds Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling 933 vials of MIC/B-COMP/(M)/CHROM/CARN Injectable due to a lack of assurance of sterility.
Product
MIC/B-COMP/(M)/CHROM/CARN, 20 mg/40 mg/50 mg/25 mcg/25 mg/mL Injectable, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0391-2017·2017-01-11
Wells Pharmacy Recalls Sermorelin Injectable Kits Due to Sterility Concerns
Wells Pharmacy is recalling Sermorelin Acetate/GHRP (2) Injectable Kits because the agency could not ensure the product was sterile.
Product
Sermorelin Acetate/GHRP (2) 9 mg/9 mg Injectable Kit, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0328-2017·2017-01-11
Wells Pharmacy Recalls Ultra-Test Injectable Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling 157 vials of Ultra-Test Injectable nationwide due to a lack of assurance of sterility.
Product
ULTRA-TEST (CYP 80%/PROP 20%) Injectable, 250 mg/mL 10 mL vial, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0853-2017·2017-01-11
Winn Dixie Mush & Garlic Herb Steak Recalled for Listeria Risk
Country Fresh Products is recalling Winn Dixie Mush & Garlic Herb Steak due to potential Listeria monocytogenes contamination.
Product
Winn Dixie, Mush & Garlic Herb Steak 7.5oz
Category
Food
Distribution
12 states
SevereFDA (Drugs)·D-0379-2017·2017-01-11
Wells Pharmacy Recalls Mitomycin Kits Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling Mitomycin 20 mg kits nationwide due to a lack of assurance of sterility.
Product
Mitomycin 20 mg Injectable, Lyophilized (Buffered), 1 mL vial, Kit, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0331-2017·2017-01-11
Wells Pharmacy Recalls Phenylephrine HCl Injectable Due to Sterility Concerns
Wells Pharmacy Network LLC is recalling 1,968 vials of Phenylephrine HCl Injectable due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Phenylephrine HCl Injectable, 1 mg/mL (0.1%), 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL
Category
Drug
Distribution
Distributed nationwide

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21776–21800 of 39678