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 deaths or serious injuries are reported, 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

10151–10175 of 36631

SevereFDA (Devices)·Z-0838-2021·2021-01-20
Fresenius Naturalyte Liquid Acid Concentrate Recalled for Conductivity Deviation
Fresenius Medical Care is recalling Naturalyte Liquid Acid concentrate bottles due to conductivity deviations and calcium concentration below manufacturing specifications.
Product
Naturalyte Liquid Acid concentrate bottles, Product Code 08-4231-0 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0227-2021·2021-01-20
Nostrum Recalls Metformin Hydrochloride Extended-Release Tablets Due to NDMA Impurity
Nostrum Laboratories is recalling Metformin Hydrochloride Extended-Release Tablets, 750 mg, because the product contains N-Nitrosodimethylamine (NDMA) above acceptable intake levels.
Product
Metformin Hydrochloride Extended-Release Tablets, USP, 750 mg, 100 tablets per bottle, Rx Only, Manufactured by: Nostrum Laboratories, Inc., Kansas City, MO 64120, NDC: 29033-056-01
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·21070·2021-01-19
Rapala Recalls Rechargeable Fillet Knives Due to Fire Hazard
Rapala USA is recalling about 128,000 rechargeable fillet knives because the batteries can overheat and catch fire if non-Rapala chargers are used.
Product
Rapala® Rechargeable Fillet Knives (Item No. RRFN)
Category
Consumer Product
Distribution
Distributed nationwide
SevereUSDA FSIS·002-2021·2021-01-15
Nestlé Prepared Foods recalls pepperoni hot pockets due to possible foreign matter contamination
The USDA Food Safety and Inspection Service is recalling approximately 762,615 pounds of not-ready-to-eat pepperoni hot pockets because they may contain glass and hard plastic fragments. One consumer reported a minor oral injury, but no additional illness cases were reported.
Product
Nestlé Prepared Foods Recalls Not-Ready-to-Eat Pepperoni Hot Pockets Product Due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0192-2021·2021-01-13
SCA Pharmaceuticals Recalls Fentanyl and Bupivacaine Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 996 fentanyl and bupivacaine syringes due to a lack of assurance of sterility and potential defective caps.
Product
fentaNYL 100 mcg/50mL Bupivacaine HCl 0.125% in 0.9% Sodium Chloride 50 mL, 50 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals,755 Rainbow Rd., Windsor, CT, 06095, barcode 70004023122
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0190-2021·2021-01-13
SCA Pharmaceuticals Recalls Esmolol Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 952 syringes of Esmolol HCl 100 mg/10 mL due to a lack of assurance of sterility and potential defective caps.
Product
Esmolol HCl 100 mg/10 mL (10mg/ mL), 10 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004062012
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0198-2021·2021-01-13
SCA Pharmaceuticals Recalls Labetalol HCl Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 9,057 syringes of labetalol HCl injection due to a lack of assurance of sterility and potential defective syringe caps.
Product
labetalol HCl 20 mg/4 mL, Injection for Intravenous Use (5mg/mL), Rx Only, 4 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004070028
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0211-2021·2021-01-13
SCA Pharmaceuticals Recalls Rocuronium Br Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 13,096 syringes of Rocuronium Br 50 mg/5mL due to a lack of assurance of sterility and potential defective caps.
Product
Rocuronium Br 50 mg/5mL (10 mg/mL), a) 5 mL Single Dose Syringe Red Label(barcode 7000485009) Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095 and b) 5 mL Single Dose Syringe White Label (barcode 70004085028), Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0196-2021·2021-01-13
Bonduelle Mixed Veg Recall Issued Due to Metal Fragment Risk
Bonduelle Canada Inc. is recalling GE Mixed Veg products because they may contain metal fragments. Consumers should stop using the product.
Product
GE Mixed Veg (4) 12/32oz/GE Mixed Veg (4) 12/32oz - packed in corrugated cases of 12 individual printed poly bags
Category
Food
Distribution
8 states
SevereFDA (Drugs)·D-0197-2021·2021-01-13
SCA Pharmaceuticals Recalls Ketamine Injection Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 11,075 syringes of Ketamine 100 mg/10mL injection due to a lack of assurance of sterility and potential defective syringe caps.
Product
Ketamine 100 mg/10mL in 0.9% Sodium Chloride Injection (10 mg/mL), CII, Rx Only, 10 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004043012
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0214-2021·2021-01-13
SCA Pharmaceuticals Recalls Fentanyl Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 6,710 fentanyl syringes distributed to hospitals nationwide due to a lack of assurance of sterility and potential defective caps.
Product
fentaNYL 100 mcg/2mL Injection for IV or IM Use, 2 mL Single Dose Syringe, CII, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095 barcode 70004020006
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0189-2021·2021-01-13
SCA Pharmaceuticals Recalls ePHEDrine Sulfate Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling 7,257 syringes of ePHEDrine Sulfate Injection due to a lack of assurance of sterility and potential defective syringe caps.
Product
ePHEDrine Sulfate 50 mg/10mL in 0.9% Sodium Chloride Injection, 10 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095 barcode 70004060412
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0199-2021·2021-01-13
SCA Pharmaceuticals Recalls Lidocaine HCl Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling Lidocaine HCl 1% syringes due to a lack of assurance of sterility and potential defective caps.
Product
Lidocaine HCl 1% 10 mL (10mg/ml), Rx Only, 1 mL Single Dose Syringe, SCA Pharma, Inc., 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004072012
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0196-2021·2021-01-13
SCA Pharmaceuticals Recalls Hydromorphone Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 1,056 hydromorphone syringes because a defective cap may compromise sterility. The product was distributed to hospitals nationwide.
Product
HYDROmorphone HCl 30 mg/30 mL in 0.9% Sodium Chloride Injection (1 mg/mL) a) 30 mL Plungerless Single Dose Syringe (barcode 70004030316) and b) 30 mL Single Dose Syringe (barcode 70004030321), Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0188-2021·2021-01-13
SCA Pharmaceuticals Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 1,879 syringes of ePHEDrine Sulfate injection due to a lack of assurance of sterility and potential defective syringe caps.
Product
ePHEDrine Sulfate, 50 mg/5mL in 0.9% Sodium Chloride Injection, 5 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004060509
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0186-2021·2021-01-13
SCA Pharmaceuticals Recalls Atropine Sulfate Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling Atropine Sulfate Injection syringes due to a lack of assurance of sterility and potential defective caps.
Product
Atropine Sulfate Injection, 0.8 mg/2 mL (0.4 mg/mL), 2 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004004006
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0775-2021·2021-01-13
Boston Scientific Recalls AXIOS Stent Delivery Systems Due to Fitting Detachment Risk
Boston Scientific is recalling 38 units of AXIOS Stent and Electrocautery delivery systems because a fitting may detach, risking peritonitis.
Product
AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm x10mm UPN: M00553660 - Product Usage: The stent is intended for implantation up to 60 days and should be removed upon confirmation of pseudocyst or walled-off necrosis resolution.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0773-2021·2021-01-13
Boston Scientific Recalls AXIOS Stent Delivery System Due to Fitting Detachment
Boston Scientific is recalling 13 units of the AXIOS Stent and Electrocautery - Enhanced Delivery System because a fitting may detach, risking peritonitis.
Product
AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x10mm UPN: M00553640 - Product Usage: The stent is intended for implantation up to 60 days and should be removed upon confirmation of pseudocyst or walled-off necrosis resolution.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0213-2021·2021-01-13
SCA Pharmaceuticals Recalls ePHEDrine Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling ePHEDrine 25 mg/5 mL Injection syringes because a defective cap may compromise sterility. The product was distributed to hospitals nationwide.
Product
ePHEDrine 25 mg/5 mL in 0.9% Sodium Chloride Injection, Rx Only, 5 mL Single Dose Syringe, SCA Pharmaceuticals 8521 Knoedl Ct., Little Rock, AR, 72205, barcode 70004060409
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0210-2021·2021-01-13
SCA Pharmaceuticals Recalls Phenylephrine Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 14,580 syringes of Phenylephrine HCl due to a lack of assurance of sterility and potential defective caps.
Product
PHENYLephrine HCl 500 mcg/5mL in 0.9% Sodium Chloride (100 mcg/mL), Rx Only, 5 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004081011
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0187-2021·2021-01-13
SCA Pharmaceuticals Recalls Buffered Lidocaine Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 3,793 syringes of Buffered Lidocaine HCl due to a potential defective cap that compromises sterility. The product was distributed to hospitals nationwide.
Product
Buffered Lidocaine HCl, 1%, 5 mL (10mg/mL) with Sodium Bicarbonate Injection for Local Anesthetic Use, 5 mL Single Dose Syringe, Rx Only SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004072509
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0200-2021·2021-01-13
American Blue Ribbon Recalls French Silk Pies Due to Undeclared Pecans
American Blue Ribbon Holdings LLC is recalling 9-inch French Silk Base pies because they contain undeclared pecans, a major food allergen.
Product
9" French Silk Base, Item 7545, Count per case 6 Ea., Case Weight 12 lb. 3 oz. UPC 50796220075458. Keep Frozen.
Category
Food
Distribution
11 states
SevereFDA (Drugs)·D-0194-2021·2021-01-13
SCA Pharmaceuticals Recalls Glycopyrrolate Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 1,614 syringes of Glycopyrrolate 1 mg/5mL due to a lack of assurance of sterility and potential defective caps.
Product
Glycopyrrolate 1 mg/5mL (0.2mg/mL), 5 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004063809
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0202-2021·2021-01-13
SCA Pharmaceuticals Recalls Morphine Sulfate Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of morphine sulfate injection syringes due to a lack of assurance of sterility and potential defective caps.
Product
morphine sulfate 150 mg/30 mL in 0.9% Sodium Chloride Injection, (5 mg/mL), Rx Only, 30 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004010316
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0206-2021·2021-01-13
SCA Pharmaceuticals Recalls Rocuronium Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 7,940 syringes of Rocuronium Br 100 mg/10mL because defective caps may compromise sterility. The product was distributed to hospitals nationwide.
Product
Rocuronium Br 100 mg/10mL (10 mg/mL), Rx Only, 10 mL Single Dose Syringe, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR, 72205, barcode 70004085012
Category
Drug
Distribution
Distributed nationwide

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10151–10175 of 36631