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

14126–14150 of 36679

SevereFDA (Devices)·Z-1268-2019·2019-05-22
Ethicon Curved Intraluminal Staplers Recalled for Insufficient Firing Stroke
Ethicon Endo-Surgery is recalling Curved Intraluminal Staplers, Model CDH25A, because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Curved Intraluminal Staplers, 25 mm diameter, Model CDH25A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1267-2019·2019-05-22
Ethicon Curved Intraluminal Staplers Recalled for Insufficient Firing Stroke
Ethicon Endo-Surgery Inc is recalling Curved Intraluminal Staplers, Model CDH21A, because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Curved Intraluminal Staplers, 21 mm diameter, Model CDH21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1281-2019·2019-05-22
Preferred Pharmaceuticals Recalls Losartan Potassium Tablets Due to Impurity
Preferred Pharmaceuticals is recalling Losartan Potassium 50mg tablets because FDA testing found an impurity above acceptable levels.
Product
Losartan Potassium Tab. USP 50mg, a) 30 count bottle (NDC 68788-0048-03) and b) 90 count bottle (NDC 68788-0048-09), Rx only, Preferred Pharmaceuticals, Inc., Anaheim, CA, Mfg: Torrent Pharma Inc., Basking Ridge, NJ
Category
Drug
Distribution
3 states
SevereFDA (Food)·F-1386-2019·2019-05-22
AmeriHerb Mullein Leaf Recalled for Potential E. coli Contamination
AmeriHerb International Inc is recalling 144 lbs of Mullein leaf due to potential E. coli contamination. The product was distributed nationwide and to Canada.
Product
Mullein leaf c/s, Verbascum Thapsus, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·19V384000·2019-05-22
Newmar Recalls 2019 Motorhomes Due to Loose Brake Caliper Bolts
Newmar is recalling 2019 Mountain Aire and Essex motorhomes because loose brake caliper mounting bolts may reduce brake effectiveness and increase crash risk.
Product
NEWMAR — NEWMAR ESSEX, MOUNTAIN AIRE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1276-2019·2019-05-22
Ethicon Endo-Surgery Recalls Straight Intraluminal Staplers Due to Firing Defect
Ethicon Endo-Surgery Inc is recalling 434,614 Straight Intraluminal Staplers (Model SDH25A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Product
Straight Intraluminal Staplers, 25 mm diameter, Model SDH25A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1388-2019·2019-05-22
AmeriHerb Goldenseal Herb Recalled for Potential E. coli Contamination
AmeriHerb International Inc is recalling 36 lbs of Goldenseal herb due to potential contamination with generic E. coli. The product was distributed nationwide and to Canada.
Product
Goldenseal herb c/s, Hydrastis Canadensis, Not for use during pregnancy, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1352-2019·2019-05-22
Molift 2-Point Sling Bar Recalled Due to Hook Breakage Risk
Moller Vital is recalling Molift 2-Point sling bars because broken hooks may cause the sling to slip and patients to fall.
Product
Molift 2-Point sling bar, an accessory for Molift Mover 180/Air. Item nos. 1830001 1830002 1830002C 1830003
Category
Medical Device
Distribution
10 states
SevereFDA (Food)·F-1342-2019·2019-05-22
FDA Orders Recall of Juices International 12-Ounce Glass Bottled Juices
Juices International is recalling 12-ounce glass bottled juices in the New York area due to a violation of a Consent Decree of Injunction.
Product
All Juice Drinks and Beverages in 12 ounce glass bottles including but not limited to Agony, Double Trouble, Front End Lifter, Irish (sea) Moss, Cashew Punch, Carrot Juice, Sorrel, Carrots & Beet, Carrot & Ginger, Ginger Beer, Pineapple Twist. Keep Refrigerated
Category
Food
Distribution
0 states
SevereUSDA FSIS·056-2019·2019-05-21
BEF Foods Recalls Bob Evans Beef Stroganoff Pasta Produced Without Inspection
BEF Foods is recalling approximately 527 pounds of Bob Evans Beef Stroganoff Pasta produced without federal inspection. No adverse reactions have been reported.
Product
BEF Foods, Inc. — BEF Foods, Inc. Recalls Beef Products Produced without Benefit of Inspection
Category
Food
Distribution
7 states
SevereCPSC·19124·2019-05-21
ION Audio Recalls Portable Speakers Due to Explosion Hazard
ION Audio is recalling four models of portable speakers because hydrogen gas can leak from the battery, causing the speaker to burst and explode.
Product
Portable speakers
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·19V383000·2019-05-21
Honda Recalls 2019 CR-V Vehicles for Steering Wheel Air Bag Defect
Honda is recalling 2019 CR-V vehicles because burrs on the steering wheel core may damage air bag wiring, potentially disabling the driver's air bag or causing it to deploy unexpectedly.
Product
HONDA — HONDA CR-V
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V381000·2019-05-20
Newmar Recalls 2019-2020 Motorhomes Due to Brake Valve Defect
Newmar is recalling 40 specific 2019 and 2020 motorhomes because a brake relay valve defect may cause extended stopping distances, increasing crash risk.
Product
NEWMAR — NEWMAR KING AIRE, LONDON AIRE, ESSEX, DUTCH STAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V380000·2019-05-19
Heil AJB9-1040 Hybrid Trailers Recalled for Frame Cracking
Entrans is recalling 2017-2020 Heil AJB9-1040 Hybrid trailers because frame cracks may develop, affecting handling and increasing crash risk.
Product
HEIL — HEIL AJB9-1040 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·055-2019·2019-05-18
Vienna Beef Recalls Frankfurters Due to Possible Metal Contamination
Vienna Beef Ltd. is recalling approximately 2,030 pounds of beef frank links that may contain metal. The products were shipped to food service locations in Illinois, Indiana, and Wisconsin.
Product
Vienna Beef Ltd. — Vienna Beef Ltd. Recalls Beef Products due to Possible Foreign Matter Contamination
Category
Food
Distribution
3 states
SevereUSDA FSIS·054-2019·2019-05-17
Caito Foods Recalls Chicken Salads Due to Undeclared Soy Allergen
Caito Foods LLC is recalling approximately 1,767 pounds of ready-to-eat chicken salads because they contain undeclared soy, a known allergen.
Product
Caito Foods, LLC — Caito Foods LLC. Recalls Salads with Chicken Products due to Misbranding and Undeclared Allergens
Category
Food
Distribution
5 states
SevereNHTSA·19V377000·2019-05-16
Suzuki Recalls 2018-2019 Burgman 200 Scooters for Transmission Defect
Suzuki is recalling 2018-2019 Burgman 200 scooters because a transmission part may break, causing loss of power and increasing crash risk.
Product
SUZUKI — SUZUKI BURGMAN 200
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V376000·2019-05-16
Micro Bird Recalls 2018-2019 School Buses for Solenoid Overheating Risk
Micro Bird is recalling 2018-2019 G5 and T-Series school buses because a heavy-duty solenoid may overheat nearby components, potentially causing vehicle stoppage or fire.
Product
MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, G5 SCHOOL BUS, T-SERIES SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1338-2019·2019-05-15
Caito Foods Recalls Fresh Cut Melons for Salmonella Carrau Risk
Caito Foods LLC is recalling fresh cut watermelon, honeydew, cantaloupe, and mixed fruit due to potential Salmonella Carrau contamination.
Product
Fresh cut watermelon, fresh cut honeydew melon, fresh cut cantaloupe and fresh cut mixed fruit containing one of these melons.
Category
Food
Distribution
0 states
CriticalFDA (Drugs)·D-1277-2019·2019-05-15
Alvogen Recalls Fentanyl Transdermal Systems Due to Product Mix-Up
Alvogen is recalling Fentanyl Transdermal Systems because a customer reported a carton labeled 12 mcg/h contained 50 mcg/h patches.
Product
FENTANYL SYSTEM — FENTANYL SYSTEM (FENTANYL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1331-2019·2019-05-15
Laduree Frozen Poppy Seed Bread Recalled for Elevated Morphine and Codeine
Laduree USA is recalling frozen poppy seed bread containing elevated levels of morphine and codeine. The product was distributed to warehouses and restaurants in Washington DC and New York.
Product
Frozen Poppy Seed Bread (57 grams), UPC Codes: (01)03556420003673(15)191122(10)181122(91)0937326, Lot 22112018
Category
Food
Distribution
4 states
SevereFDA (Drugs)·D-1272-2019·2019-05-15
Zydus Recalls Acyclovir Tablets Due to Labeling Error with Carvedilol
Zydus Pharmaceuticals is recalling Acyclovir 400 mg tablets because one bottle was found to contain Carvedilol 6.25 mg tablets due to a label mix-up.
Product
ACYCLOVIR — ACYCLOVIR (ACYCLOVIR)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·19V374000·2019-05-15
Navistar Recalls 2017 IC CE Transit Buses for Brake Drag
Navistar is recalling 2017 IC CE transit buses because the driver-side rear brakes may drag, posing a fire and injury risk.
Product
IC BUS — IC BUS CESB, CE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1296-2019·2019-05-15
Abbott ARCHITECT cSystems ICT Module Recall for False Chloride Results
Abbott is recalling ARCHITECT cSystems ICT Modules due to a potential for falsely elevated serum or plasma chloride results.
Product
Abbott ARCHITECT cSystems ICT Module, REF 09D28-03. Product Usage: The ARCHITECT cSystems ICT (Integrated Chip Technology) is used for the quantitation of sodium, potassium, and chloride in human serum, plasma, or urine.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V373000·2019-05-15
Navistar Recalls IC Bus School Buses Due to Rear Brake Drag
Navistar is recalling 2016-2020 IC Bus school buses because the driver-side rear brakes may drag, potentially causing fire or injury.
Product
IC BUS — IC BUS RECB, CE, CESB, RESB
Category
Vehicle
Distribution
Distributed nationwide

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14126–14150 of 36679