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

16501–16525 of 39596

SevereFDA (Drugs)·D-0359-2019·2018-12-05
Sandoz Losartan Potassium and Hydrochlorothiazide Tablets Recalled for NDEA Impurity
Sandoz is recalling Losartan Potassium and Hydrochlorothiazide tablets because FDA testing found the impurity NDEA above acceptable levels.
Product
Sandoz Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 1000-count bottles, Rx Only, Finished Drug Product Manufactured by: Lek Pharmaceuticals d.d. SI-1526 Ljubljana,Sovenia for Sandoz Inc., Princeton, NJ 08540, NDC 0781-5207-10.
Category
Drug
Distribution
2 states
SevereFDA (Food)·F-0723-2019·2018-12-05
Chukar Cherry Company Recalls Organic Chocolate Rainier Cherries for Unlabeled Milk
Chukar Cherry Company is recalling 502 pouches of Organic Ultra Dark Vanilla Chocolate Rainier Cherries because the product contains milk, which is not listed on the label.
Product
Organic Ultra Dark Vanilla Chocolate Rainier Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261 27207 5. The label is read in parts: "***ORGANIC ULTRA DARK VANILLA CHOCOLATE RAINIER CHERRIES *** Ingredients: Organic Bittersweet Chocolate…
Category
Food
Distribution
22 states
SevereFDA (Devices)·Z-0437-2019·2018-12-05
Maquet Cardiovascular Recalls QUADROX-i Neonatal Membrane Oxygenators
Maquet Cardiovascular is recalling QUADROX-i Neonatal membrane oxygenators due to a potential for blood leakage at the blood inlet connector when using a specific reducing screw adapter.
Product
QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO 11000-USA#QUADROX-i Neo.+Reservoir), Part Number 701055207 The membrane oxygenator QUADROXi Neonatal is intended for use in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0502-2019·2018-12-05
NxStage PureFlow B Solution Recalled for Potential Bag Bursting and Injury
NxStage Medical is recalling specific lots of PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.
Product
NxStage PureFlow B Solution-RFP-402, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0505-2019·2018-12-05
NxStage PureFlow B Solution Recalled for Potential Bag Bursting
NxStage Medical is recalling PureFlow B Solution because the bag's smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.
Product
NxStage PureFlow B Solution-RFP-406, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0721-2019·2018-12-05
Chukar Cherry Company Recalls Ultra Dark Chocolate Black Forest Cherries
Chukar Cherry Company is recalling Ultra Dark Chocolate Black Forest Cherries due to the unintentional presence of milk, which is not listed on the label.
Product
Ultra Dark Chocolate Black Forest Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261 23907 8. The label is read in parts: "***ULTRA DARK CHOCOLATE BLACK FOREST CHERRIES***Ingredients: Bittersweet Chocolate (Cacao Beans, Pure Cane Sugar…
Category
Food
Distribution
22 states
SevereFDA (Food)·F-0679-2019·2018-12-05
Purveyors Kitchen Pumpkin Pesto Tapenade Recalled for Undeclared Walnut Allergen
Nor Cal Food Solutions LLC is recalling Purveyors Kitchen Pumpkin Pesto Tapenade because the product does not declare walnuts as an ingredient or allergen.
Product
Purveyors Kitchen Pumpkin Pesto Tapenade; NET WT 7.75 oz. (220G) UPC: 0 37677 01624 9 Ingredients: Water, Pumpkin, Basil, Parsley, Canola Oil, Sugar, Garlic, Parmesan Cheese (pasteurized skim milk, cultures, salt, enzymes), Lemon juice [concentrate], Sea Salt, Spices.…
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-0436-2019·2018-12-05
Maquet QUADROX-i Neonatal Membrane Oxygenator Recalled for Blood Leakage Risk
Maquet is recalling QUADROX-i Neonatal membrane oxygenators because a specific reducing screw adapter may cause blood leakage at the inlet connector.
Product
QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO 10000-USA#QUADROX-i Neo.+Reservoir), Part Number 701055120 The membrane oxygenator QUADROXi Neonatal is intended for use in extracorporeal circulation during cardiopulmonary bypass in cardiac surgery.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18V863000·2018-12-05
Volkswagen Recalls 2018 Audi Models for Fuel Hose Fire Risk
Volkswagen is recalling 2018 Audi A3 and TT models because a fuel hose connector may detach, causing a leak that increases fire risk.
Product
AUDI — AUDI A3 CABRIOLET, TT ROADSTER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E112000·2018-12-05
Cummins Recalls ISV5.0 Diesel Engines Due to Air Compressor Belt Slip
Cummins is recalling ISV5.0 diesel engines because a slipping air compressor belt can reduce braking performance, increasing crash risk.
Product
ENGINE AND ENGINE COOLING:ENGINE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V859000·2018-12-04
Newmar Recalls 2018-2019 Motorhomes Due to Loose Brake Caliper Bolts
Newmar is recalling 2018-2019 Essex, Ventana, and London Aire motorhomes because brake caliper mounting bolts may be loose, increasing crash risk.
Product
NEWMAR — NEWMAR VENTANA LE, VENTANA, ESSEX, LONDON AIRE
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·19043·2018-12-04
Signature Hardware Recalls Wall-Mounted Shower Seats Due to Fall and Laceration Hazards
Signature Hardware is recalling wall-mounted shower seats because corroding aluminum hardware can cause falls and lacerations. Consumers should stop using the seats and contact the company for a refund.
Product
Wall-mounted shower seats
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·18V860000·2018-12-04
Yamaha Recalls 2015-2016 YZFR3 Motorcycles for Shift Shaft Spring Defect
Yamaha is recalling 2015-2016 YZFR3 motorcycles because a shift shaft torsion spring may fracture, causing difficulty shifting gears and increasing crash risk.
Product
YAMAHA — YAMAHA YZFR3
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·085-2018 EXP·2018-12-04
JBS Tolleson Recalls Raw Beef Products Due to Salmonella Newport
JBS Tolleson is recalling approximately 12.1 million pounds of raw beef products, including ground beef, due to possible Salmonella Newport contamination.
Product
JBS Tolleson Inc. — JBS Tolleson, Inc. Recalls Raw Beef Products due to Possible Salmonella Newport Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·18V857000·2018-12-03
Gulf Stream Vintage Cruiser Recalled for Insufficient Bearing Grease
Gulf Stream is recalling 2019 Vintage Cruiser recreational trailers because inner hub bearings may lack sufficient grease, risking overheating and hub failure.
Product
GULF STREAM — GULF STREAM VINTAGE CRUISER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V858000·2018-12-03
McNeilus and Oshkosh Trucks Recalled for CNG Valve Defect
McNeilus is recalling 2016-2018 trucks and Oshkosh S-Series vehicles because a CNG fuel tank valve stem may eject, posing injury and fire risks.
Product
OSHKOSH — OSHKOSH, MCNEILUS S-SERIES, XE REAR LOADER, STANDARD MIXER, BRIDGEMASTER V MIXER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E111000·2018-12-01
Luxfer Recalls One-Turn Valves Due to Potential Stem Ejection Risk
Luxfer Canada Ltd. is recalling One-Turn Valves (part number MPVE-250) because the valve stem may forcibly eject if the knob is turned more than one turn, posing injury and fire risks.
Product
FUEL SYSTEM, OTHER recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V854000·2018-11-30
Ducati Recalls 2018-2019 Panigale V4 Motorcycles for Timing Chain Tensioner Defect
Ducati is recalling 2018-2019 Panigale V4 motorcycles because a timing chain tensioner may loosen, causing an oil leak that increases crash risk.
Product
DUCATI — DUCATI PANIGALE V4
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V853000·2018-11-30
Keystone Recalls 2019 Montana Trailers Due to Axle Weld Defects
Keystone RV Company is recalling 2019 Montana recreational trailers because defective axle welds could cause the wheel assembly to detach, increasing crash risk.
Product
KEYSTONE — KEYSTONE MONTANA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V850000·2018-11-29
Mercedes-Benz Recalls Vehicles Due to Steering Rack Locknut Failure Risk
Mercedes-Benz is recalling specific 2015-2019 models because a steering rack locknut may break, causing the steering to stick and increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ C 350 E, E 300, C 300, CLS 450
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0657-2019·2018-11-28
Sprout Creek Farm Recalls Margie Cheese Contaminated with Listeria monocytogenes
Sprout Creek Farm, Inc. is recalling Margie Cheese wheels contaminated with Listeria monocytogenes. The recall affects one-pound wheels sold in New York.
Product
Margie Cheese. It is packaged with a green round label, wrapped in white milk paper in one-pound wheels.
Category
Food
Distribution
1 state
CriticalFDA (Food)·F-0652-2019·2018-11-28
Bazzini Pistachios Recalled Due to Salmonella Contamination
Bazzini LLC is recalling specific lots of roasted and salted in-shell pistachios because the product tested positive for Salmonella.
Product
BAZZINIS ROASTED & SALTED IN-SHELL PISTACHIOS RAMS HEAD NATURAL 16 OZ BAG UPC #0 75062 00536 2 THE BAGS ARE RED, WHITE AND BLUE.
Category
Food
Distribution
12 states
CriticalFDA (Food)·F-0651-2019·2018-11-28
Bazzini Roasted Pistachios Recalled Due to Salmonella Contamination
Bazzini LLC is recalling 25 lb boxes of roasted and salted in-shell pistachios because the product tested positive for Salmonella.
Product
BAZZINI S ROASTED & SALTED IN-SHELL SUPER COLOSSAL PISTACHIOS 25 LB BULK BOX UPC #0 75062 30700 8
Category
Food
Distribution
12 states
SevereFDA (Drugs)·D-0269-2019·2018-11-28
Sciegen Recalls Irbesartan Tablets Due to NDEA Impurity
Sciegen Pharmaceuticals is recalling Irbesartan 300mg tablets because FDA testing found the impurity N-nitrosodimethylamine (NDEA).
Product
Westminister Irbesartan Tablets, USP, 300mg, Rx Only,(a) 30-count bottle (NDC 69367-121-01, (b) 90-count bottle (NDC 69367-121-03), Manufactured by ScieGen Pharmaceuticals Inc. Hauppauge, NY 11755. Manufactured for Westminster Pharmaceuticals LLC Olive Branch, MS 20854 Made in…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0653-2019·2018-11-28
Bazzini Pistachios Recalled Due to Salmonella Contamination
Bazzini LLC is recalling specific lots of roasted and salted in-shell pistachios because the product tested positive for Salmonella.
Product
BAZZINI S ROASTED & SALTED IN-SHELL PISTACHIOS COLOSSAL NATURAL 16 OZ BAG UPC #0 75062 00535 5 THE BAGS ARE RED, WHITE AND BLUE.
Category
Food
Distribution
12 states

How to read this listing

Filters

16501–16525 of 39596