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

17276–17300 of 39601

SevereFDA (Drugs)·D-1143-2018·2018-09-05
Torrent Pharma Recalls Amlodipine, Valsartan, and Hydrochlorothiazide Tablets Due to Impurity
Torrent Pharma Inc. is recalling specific batches of Amlodipine, Valsartan, and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
Amlodipine, Valsartan and Hydrochlorothiazide Tablets, USP, 10 mg/160 mg/12.5 mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-327-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1140-2018·2018-09-05
Torrent Pharma Recalls Amlodipine and Valsartan Tablets Due to Carcinogen Impurity
Torrent Pharma Inc. is recalling specific batches of Amlodipine and Valsartan Tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
Amlodipine and Valsartan Tablets, USP, 5 mg/160 mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-207-30
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V590000·2018-09-05
Fabform Recalls 2017-2018 Power Tilt Dump Trailers Due to Hinge Fracture Risk
Fabform is recalling 2017-2018 Power Tilt dump trailers because welded hinges may fracture, causing the dump box to fall unexpectedly and increasing the risk of injury or death.
Product
FABFORM — FABFORM POWER TILT DUMP TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1147-2018·2018-09-05
Pharmcore Recalls Human Chorionic Gonadotropin Vials Due to Sterility Concerns
Pharmcore Inc. is recalling 5,718 vials of Human Chorionic Gonadotropin 5000 IU due to a lack of assurance of sterility.
Product
Human Chorionic Gonadotropin 5000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1163-2018·2018-09-05
Auro Pharmacies Recalls Testosterone Injectable Due to Sterility Concerns
Auro Pharmacies is recalling 43 vials of Testosterone Cypionate/Enanthate injectable because inadequate processes and equipment failed to assure product sterility.
Product
Testosterone Cypionate/Enanthate injectable, 126/54 mg/mL, packaged in a) 3 mL and b) 5 mL Multiple Dose vials, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1156-2018·2018-09-05
Auro Pharmacies Recalls CoEnzyme-Q10 Injectable Due to Sterility Concerns
Auro Pharmacies is recalling 39 vials of CoEnzyme-Q10 injectable because inadequate processes and equipment failed to assure product sterility.
Product
CoEnzyme-Q10 injectable, 20 mg/mL, 10 mL Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1138-2018·2018-09-05
Torrent Pharma Recalls Amlodipine and Valsartan Tablets Due to Impurity
Torrent Pharma Inc. is recalling Amlodipine and Valsartan Tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
Amlodipine and Valsartan Tablets, USP, 5 mg/320 mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-205-30
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V589000·2018-09-05
Volvo Recalls 2019 XC60 Hybrid Vehicles Due to Charging System Fire Risk
Volvo is recalling 2019 XC60 hybrid vehicles because capacitors in certain charging systems may fail, posing a shock or fire hazard.
Product
VOLVO — VOLVO XC60
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2926-2018·2018-09-05
Stanbio AC Power Adapter Recall for HemoPoint H2 Meter
Stanbio Laboratory is recalling AC power adapters for the HemoPoint H2 meter because the adapter plate may crack or detach, exposing live electrical contacts.
Product
Stanbio AC power adapter for the HemoPoint H2 meter, Model G3000 series. The firm name on the label for the HemoPoint H2 shows Manufactured by EKF-diagnostic GmbH, Germany.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1149-2018·2018-09-05
Pharmcore Recalls Human Chorionic Gonadotropin Vials Due to Sterility Concerns
Pharmcore Inc. is recalling 355 vials of Human Chorionic Gonadotropin 20000 IU due to a lack of assurance of sterility.
Product
Human Chorionic Gonadotropin 20000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1148-2018·2018-09-05
Pharmcore Recalls Human Chorionic Gonadotropin Vials Due to Sterility Concerns
Pharmcore Inc. is recalling 864 vials of Human Chorionic Gonadotropin 11000 IU due to a lack of assurance of sterility. The affected lots were distributed nationwide.
Product
Human Chorionic Gonadotropin 11000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1133-2018·2018-09-05
AvKARE Recalls Valsartan Tablets Due to Carcinogen Impurity
AvKARE Inc. is recalling Valsartan Tablets 320 mg because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
Valsartan Tablets, USP 320 mg Rx Only 30 Tablets (6x5) Unit Dose NDC 50268-786-13 Manufactured for: AvKARE, Inc. Pulaski, TN 38478
Category
Drug
Distribution
Distributed nationwide
SevereUSDA FSIS·076-2018·2018-09-05
Wayne Farms Recalls Frozen Chicken Products Due to Metal Contamination
Wayne Farms is recalling approximately 438,960 pounds of frozen, fully cooked chicken products that may contain metal pieces. Consumers are advised not to consume these items.
Product
Wayne Farms LLC — Wayne Farms, LLC Recalls Fully Cooked Chicken Products due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1906-2018·2018-09-05
Coca-Cola Recalls Minute Maid Tropical Blend Juice Due to Glass
The Coca-Cola Company is recalling 432 bottles of Minute Maid Tropical Blend juice because foreign matter believed to be glass was found in retained samples.
Product
Consumer Packaging (PET bottle): Minute Maid TROPICAL BLEND Flavored Juice Beverage 12 FL OZ (355mL), JAN0719NPA, UPC: 0 25000 06229 2. Master Case: packaged 24/12 fl.oz., GTIN number 00025000062414 (no UPC)
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-1130-2018·2018-09-05
AvKARE Recalls Valsartan Tablets Due to Carcinogen Impurity in API
AvKARE is recalling Valsartan Tablets 40 mg because a carcinogen impurity was detected in the active pharmaceutical ingredient used to manufacture the drug.
Product
Valsartan Tablets, USP 40 mg Rx Only NDC 50268-783-15 50 Tablets (5x10) Unit Dose Manufactured for: AvKARE, Inc. Pulaski, TN 38478
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1157-2018·2018-09-05
Auro Pharmacies Recalls Calcium Gluconate Injectable Due to Sterility Concerns
Auro Pharmacies is recalling 167 vials of Calcium Gluconate injectable because processes and equipment were inadequate to assure sterility.
Product
Calcium Gluconate injectable, 10%, 50 ml Single Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1165-2018·2018-09-05
Auro Pharmacies Recalls Testosterone Enanthate/Cypionate Injectable Due to Sterility Concerns
Auro Pharmacies is recalling 11 vials of Testosterone Enanthate/Cypionate injectable because the manufacturer could not assure the sterility of the product.
Product
Testosterone Enanthate/Cypionate injectable, 126/54 mg/mL, packaged in a) 3 mL and b) 5 mL Multiple Dose vials, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1852-2018·2018-09-05
Marsee Foods Recalls Cafe YUMM! Chocolate Chip Cookies for Undeclared Peanuts
Marsee Foods Inc is recalling Cafe YUMM! Chocolate Chip Cookies because they may contain undeclared peanuts. The cookies were sold at Cafe Yumm! restaurants in Oregon and Washington.
Product
Chocolate Chip Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains two boxes and each box contains 24 cookies. The master case is taped shut and labeled with the contents and production date, along with a lot code. The…
Category
Food
Distribution
2 states
SevereFDA (Drugs)·D-1161-2018·2018-09-05
Auro Pharmacies Recalls Methyl-Cobalamin Injectable Due to Sterility Concerns
Auro Pharmacies, Inc. is recalling 90 vials of Methyl-Cobalamin injectable because inadequate processes and equipment were used to assure sterility.
Product
Methyl-Cobalamin injectable, 5 mg/mL, 30 mL Multiple Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1151-2018·2018-09-05
Pharmcore Recalls Human Chorionic Gonadotropin Vials Due to Sterility Concerns
Pharmcore Inc. is recalling 2,085 vials of Human Chorionic Gonadotropin 4000 IU nationwide due to a lack of assurance of sterility.
Product
Human Chorionic Gonadotropin 4000 IU Vial Lyophilized 1109 East Hallandale Beach Blvd. Hallandale Beach, FL 33009
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1158-2018·2018-09-05
Auro Pharmacies Recalls Dexpanthenol Injectable Vials Due to Sterility Concerns
Auro Pharmacies, Inc. is recalling 91 vials of Dexpanthenol injectable due to inadequate processes and equipment to assure sterility.
Product
Dexpanthenol injectable, 250 mg/mL, 10 mL Single Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1137-2018·2018-09-05
Torrent Pharma Recalls Amlodipine and Valsartan Tablets Due to Carcinogen Impurity
Torrent Pharma Inc. is recalling Amlodipine and Valsartan Tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
Amlodipine and Valsartan Tablets, USP, 10 mg/320 mg, 30 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-204-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1131-2018·2018-09-05
AvKARE Recalls Valsartan Tablets Due to Carcinogen Impurity
AvKARE is recalling specific lots of Valsartan 80 mg tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
Valsartan Tablets, USP 80 mg Rx Only 50 Tablets (5x10) Unit Dose NDC 50268-784-15 Manufactured for: AvKARE, Inc. Pulaski, TN 38478
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1134-2018·2018-09-05
Torrent Pharma Recalls Valsartan Tablets Due to Carcinogen Impurity
Torrent Pharma Inc. is recalling specific batches of Valsartan Tablets USP, 80mg, because a carcinogen impurity was detected in the active pharmaceutical ingredient.
Product
Valsartan Tablets USP, 80mg, 90 tablets per bottle, Rx Only, Manufactured by: Torrent Pharmaceuticals LTD., Indrad-382 721, India. NDC: 13668-068-90
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2878-2018·2018-09-05
Biosense Webster Recalls WaveCrest Left Atrial Appendage Occlusion System Devices
Biosense Webster is recalling 25 units of the WaveCrest Left Atrial Appendage Occlusion System (32 mm) because the delivery sheath may buckle during recapture.
Product
WaveCrest Left Atrial Appendage (LAA), Occlusion System (32 mm), Catalog Numbers WCR1523 and WCR2523.
Category
Medical Device
Distribution
0 states

How to read this listing

Filters

17276–17300 of 39601