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

30301–30325 of 39756

SevereFDA (Devices)·Z-0016-2015·2014-10-15
Richard-Allan Scientific Recalls 10% Neutral Buffered Formalin Due to Concentration Issues
Richard-Allan Scientific is recalling 199 cases of 10% Neutral Buffered Formalin because the chemical concentration may be outside of desired specifications.
Product
Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0018-2015·2014-10-15
Cardinal Health Prefilled Buffered 10% Formalin Recalled for Concentration Issues
Richard-Allan Scientific Company is recalling Cardinal Health Prefilled Buffered 10% Formalin because the formalin concentration may be outside specifications.
Product
Cardinal Health Prefilled Buffered 10% Formalin. Product Usage:10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0006-2015·2014-10-15
Janssen Recalls Xarelto Tablets Due to Microbial Contamination
Janssen Ortho L.L.C. is recalling 13,500 bottles of Xarelto (rivaroxaban) 15 mg tablets due to confirmed microbial contamination in a sales sample.
Product
Xarelto (rivaroxaban) Tablets 15 mg per tablet, 5 count bottle, Rx Only, Manufactured by: JOLLC, Gurabo, PR 00778 NDC 50458-578-99
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0012-2015·2014-10-15
Richard-Allan Scientific Recalls Protocol 10% NBF Tissue Fixative
Richard-Allan Scientific is recalling 175 cases of Protocol 10% NBF tissue fixative because the concentration may be outside specifications.
Product
Protocol 10% NBF Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0005-2015·2014-10-15
Publix Jalapeno Bagels Recalled for Potential Glass and Stone Contamination
Publix Super Markets is recalling Jalapeno Bagels sold in Alabama, Florida, Georgia, and South Carolina because they may contain pieces of glass and small stones.
Product
Publix brand Jalapeno Bagels, sold in self service bins and counter sales.
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-0058-2015·2014-10-15
Biomet Recalls Mamba Disposable Nitinol Needles Due to Breakage Risk
Biomet is recalling 164 Mamba Disposable Nitinol Needles because high friction may cause the needles to break during use.
Product
Mamba Disposable Nitinol Needle. The Biomet Sports Medicine Mamba instruments are utilized to aid in passing suture through soft tissue. The Mamba Needle is designed for use with the Mamba Suture Passer. The needles are sterile, disposable, and for single-patient use only.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0003-2015·2014-10-15
Brilliant Cake Biscuits Recalled for Undeclared Eggs and Unapproved Colors
Domega NY International Co Ltd is recalling Brilliant Cake with Filling Milk (Biscuits) due to undeclared eggs and unapproved food colors.
Product
Brilliant Cake with Filling Milk (Biscuits), NET WT 13.9 oz (396 g), UPC 6 908166 500140, Product of China --- The product is packed in a plastic wrapped package.
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-0007-2015·2014-10-15
Zydus Recalls Atenolol Tablets Due to Superpotent Drug Complaint
Zydus Pharmaceuticals is recalling 5,400 bottles of Atenolol 25 mg tablets nationwide after a pharmacist reported that several tablets appeared noticeably thicker.
Product
ATENOLOL — ATENOLOL (ATENOLOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0009-2015·2014-10-15
Mylan Recalls Metoprolol Succinate Tablets Due to Foreign Object Presence
Mylan Pharmaceuticals is recalling 15,966 bottles of Metoprolol Succinate Extended-release Tablets 50mg because a pharmacist reported finding a rogue tablet of different size and markings in a bottle.
Product
Metoprolol Succinate Extended-release Tablets, USP 50mg, 90-count Bottles, Rx only, Mfg by Mylan Pharmaceuticals, Inc. Morgantown, WV 26505. NDC 0378-4596-77.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0018-2015·2014-10-15
SABA ACE Appetite Control Energy Recalled for DMAA Presence
AMS Health Sciences is recalling SABA ACE products manufactured before September 2013 due to the presence of DMAA.
Product
saba; ACE; Appetite Control Energy; 052234; 07/2015; Distributed by Saba; 711 NE 39th Street, Oklahoma City, OK 73105
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0002-2015·2014-10-15
Starway Inc. Recalls Peony Mark Roasted and Salted Pumpkin Seeds
Starway Inc. is recalling Peony Mark brand roasted and salted pumpkin seeds due to undeclared sulfites. The product was distributed in New York, New Jersey, Massachusetts, and Michigan.
Product
PEONY MARK brand ROASTED AND SALTED PUMPKIN SEED, NET WT. 12 oz. (340 gm), Barcode 6 932692 225765, PRODUCT OF CHINA --- PACKED FOR: STARWAY INC 137 GRATTAN STREET, BROOKLYN, NEW YORK 11237 --- NUTRITION FACTS: Serving Size 1 oz., Servings per container 12
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-0014-2015·2014-10-15
Richard-Allan Scientific Recalls 10% Neutral Buffered Formalin Due to Concentration Issues
Richard-Allan Scientific is recalling 10% Neutral Buffered Formalin because the concentration may be outside specifications. The product is used to fixate tissue for histological examination.
Product
Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10% NBF is used to store and fixate tissue prior to grossing and histological examination. It is a primary fixative that prevents autolysis (degradation) of tissue.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·14V644000·2014-10-14
Yamaha Recalls 2014 YZF-R6 Motorcycles Due to Wheel Hardness Defect
Yamaha is recalling 2014 YZF-R6 motorcycles because front and rear wheels may have insufficient hardness, increasing crash risk.
Product
YAMAHA — YAMAHA YZFR6
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·069-2014·2014-10-14
Italian Style Wedding Soup Recalled for Undeclared Soy and Egg Allergens
Fresh Food Manufacturing is recalling 1,008 pounds of Italian Style Wedding Soup because the label failed to declare soy and egg allergens.
Product
Fresh Food Manufacturing Company — Pennsylvania Firm Recalls Italian Style Wedding Soup Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
2 states
SevereNHTSA·14V643000·2014-10-14
Chrysler Recalls 2014 Dodge Durango and Jeep Grand Cherokee for Airbag Fault
Chrysler is recalling 2014 Dodge Durango and Jeep Grand Cherokee vehicles because a module fault may disable airbags and seat belt pretensioners, increasing injury risk in crashes.
Product
DODGE — DODGE, JEEP DURANGO, GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V646000·2014-10-14
Vermeer Recalls 2014 TR620 Trailers Due to Hitch Mount Defect
Vermeer is recalling 2014 TR620 Trommel trailers because an incorrect material in the pintle hitch mount may allow bolts to loosen, increasing crash risk.
Product
VERMEER — VERMEER TR620
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·067-2014-EXP·2014-10-13
Galant Food Company Recalls Additional Beef Piroshki Due to Processing Flaw
Galant Food Company is recalling an additional 130 pounds of beef piroshki because the meat filling did not reach the required cooking temperature.
Product
Galant Food Co — California Firm Expands Recall of Beef Products Due To Possible Processing Flaw
Category
Food
Distribution
1 state
SevereNHTSA·14V638000·2014-10-10
Strick Dry Freight Van Trailers Recalled for Rear Impact Guard Defect
Strick Trailers is recalling 2009-2015 Dry Freight Van Trailers because rear impact guards do not meet federal safety standards, increasing injury risk in crashes.
Product
STRICK — STRICK DRY FREIGHT VAN TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V642000·2014-10-10
Wheeled Coach Recalls Ambulances Due to Suspension Tank Mount Failure Risk
Wheeled Coach is recalling certain 2013-2015 ambulances because a suspension fluid tank mount may fail, causing the tank to separate and create a road hazard.
Product
WHEELED COACH — WHEELED COACH TYPE III AMBULANCE, TYPE I AMBULANCE
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1613-2014·2014-10-08
Black Ant capsules recalled for undeclared sildenafil
Eugene Oregon, Inc. is recalling Black Ant capsules because FDA testing found undeclared sildenafil. The product was marketed without an approved NDA or ANDA.
Product
Black Ant, 2800 mg, four capsules per box, Manufacturer Qinghai Baojiantang Pharmaceutical Co., Ltd.
Category
Drug
Distribution
11 states
CriticalFDA (Drugs)·D-1610-2014·2014-10-08
Baxter Recalls Dianeal Low Calcium Peritoneal Dialysis Solution Bags
Baxter Healthcare is recalling 50,530 bags of Dianeal Low Calcium peritoneal dialysis solution due to the presence of particulate matter found during manufacturing.
Product
DIANEAL LOW CALCIUM WITH DEXTROSE — DIANEAL LOW CALCIUM WITH DEXTROSE (SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Food)·F-2534-2014·2014-10-08
Boskovich Farms Recalls Diced Roma Tomatoes Due to Salmonella Risk
Boskovich Farms is recalling diced Roma tomatoes sold in 24-ounce bags because they may be contaminated with Salmonella.
Product
2/24 ounce clear plastic bags of 3/8 inch diced Roma tomatoes. These bags are in a cardboard carton. The bags and carton have a yellow label that reads in part: Boskovich Farms, Inc Costco Deli Dept. 63 ***QUINOA SALAD KIT Item # 624843 CONTENTS: (2) QUINIA MIX *** (2) Diced…
Category
Food
Distribution
1 state
CriticalFDA (Drugs)·D1612-2014·2014-10-08
African Black Ant capsules recalled for undeclared sildenafil
Eugene Oregon, Inc. is recalling African Black Ant capsules because FDA laboratory analyses found undeclared sildenafil. The product was marketed without an approved NDA/ANDA.
Product
AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongwei Bioengineering Company, No. 158, Renmin Road, Xining City.
Category
Drug
Distribution
11 states
CriticalFDA (Food)·F-2539-2014·2014-10-08
TJ's Place Recalls Basil Pesto Pasta Due to Listeria Risk
TJ's Place is recalling 8 oz. Basil Pesto Pasta tubs because they may be contaminated with Listeria monocytogenes.
Product
Basil Pesto Pasta packaged in a non-flex plastic tub, net wt 8 oz. A green sticker is placed on the lid of the package which contains the lot code. Product is refrigerated
Category
Food
Distribution
1 state
CriticalFDA (Drugs)·D-1614-2014·2014-10-08
MOJO RISEN Recalled for Undeclared Sildenafil and Lack of Approval
Eugene Oregon, Inc. is recalling MOJO RISEN because FDA testing found undeclared sildenafil and the product was marketed without an approved NDA or ANDA.
Product
MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville, UT 84663
Category
Drug
Distribution
11 states

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30301–30325 of 39756