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

24401–24425 of 39708

SevereFDA (Drugs)·D-0872-2016·2016-06-01
Sanofi Recalls Auvi-Q Epinephrine Auto-Injectors Due to Defective Delivery System
Sanofi-Aventis is recalling Auvi-Q epinephrine auto-injectors because a defective delivery system may result in inaccurate dosage delivery.
Product
Auvi-Q (epinephrine injection, USP) Auto-Injector, 0.3 mg (a) 2 prefilled auto injectors + 1 trainer (NDC 0025-5833-02) and (b) 1 prefilled auto injector + 1 trainer (NDC 0024-5833-00), Rx Only, Manufactured for Sanofi-Aventis US, LLC Bridgewater, NJ 08807 A Sanofi Company
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0859-2016·2016-06-01
Teva Recalls Amikacin Sulfate Injection Due to Glass Particulate Matter
Teva Pharmaceuticals USA is recalling Amikacin Sulfate injection vials because glass particulate matter was identified in one vial.
Product
Amikacin Sulfate injection USP,1 gm/4 mL (250 mg/mL) 4mL vial, Rx only, Manufactured in Hungary For: Teva Pharmaceuticals USA, INC. North Wales, PA 19454. Individual Pack NDC 0703-9040-01, Shelf Pack NDC 0703-9040-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1384-2016·2016-06-01
Unlabeled Dried Yellow Fish Recalled for Being Uneviscerated
WD Import and Export Inc. is recalling 2 cases of unlabeled, whole dried yellow fish from China found to be uneviscerated.
Product
Whole Dried Yellow Fish in bulk cardboard box, unlabeled, Product of China --- Fish measured 6.5 - 7.5 inches in length
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-1823-2016·2016-06-01
Biomet Recalls Trauma and Sports Medicine Instruments Due to Seal Defects
Biomet, Inc. is recalling specific trauma and sports medicine instruments and implants because insufficient seal strength on sterile packaging could compromise sterility and lead to infection.
Product
Various trauma and sports medicine instruments and implants. Screw, fixation, bone.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0866-2016·2016-06-01
Fresenius Kabi Recalls Octreotide Acetate Injection Due to Impurities
Fresenius Kabi is recalling specific lots of Octreotide Acetate Injection because they failed impurities and degradation specifications.
Product
OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius Kabi USA, LLC, Schaumburg, IL 60173, NDC 63323-365-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0902-2016·2016-06-01
FDA Recalls Mojo Risen Distributed Without Approved New Drug Application
R Thomas Marketing, LLC is recalling Mojo Risen capsules nationwide because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Mojo Risen, packaged in BIG BOX (24 individual cards / 2 capsules per card/ 48 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0898-2016·2016-06-01
Happy Passengers Recalled for Lack of FDA Approval
R Thomas Marketing, LLC is recalling Happy Passengers capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Happy Passengers, packaged in BIG BOX (30 small boxes / 1 capsule per box / 30 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
CriticalNHTSA·16V384000·2016-05-31
Ford Recalls Vehicles Due to Air Bag Inflator Rupture Risk
Ford is recalling specific 2005-2011 vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Product
FORD — FORD, MERCURY, LINCOLN MUSTANG, FORD GT, FUSION, MILAN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16E050000·2016-05-31
Stanley and Mac Data Torq Air-Impact Wrenches Recalled for Software Error
Stanley Assembly Technologies is recalling specific air-impact wrenches with a software error that may cause over-tightening of vehicle lug nuts, increasing crash risk.
Product
EQUIPMENT recall
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·16V385000·2016-05-31
Winnebago Recalls 2015-2016 Motor Homes for Steering Box Defect
Winnebago is recalling 2015-2016 Tour and Itasca Ellipse motor homes because a steering box defect could cause loss of steering ability.
Product
WINNEBAGO — WINNEBAGO, ITASCA TOUR, ELLIPSE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16E049000·2016-05-27
Xperion Recalls CNG Fuel Tanks Due to Leak Risk
Xperion is recalling specific CNG fuel tanks because a neck adapter may pull out, allowing fuel to leak and increasing fire risk.
Product
FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V377000·2016-05-27
Forest River Recalls 2015-2016 Glaval Concorde Buses for Parking Brake Defect
Forest River is recalling 2015-2016 Glaval Concorde and Concorde II buses because a parking brake cable clip may fail, causing the vehicle to roll unexpectedly.
Product
GLAVAL BUS — GLAVAL BUS CONCORDE II, CONCORDE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V373000·2016-05-27
Jaguar Recalls 2009-2011 XF Models for Air Bag Inflator Rupture Risk
Jaguar is recalling 2009-2011 XF vehicles in specific states because passenger air bag inflators may rupture during a crash, potentially causing serious injury or death.
Product
JAGUAR — JAGUAR XF
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V376000·2016-05-27
Audi Recalls 2008-2009 A4, A5, and Q5 for Air Bag Control Unit Defect
Volkswagen Group of America is recalling 2008-2009 Audi A4, A5, and Q5 vehicles because the air bag control units may corrode and fail, potentially preventing air bag deployment in a crash.
Product
AUDI — AUDI Q5, A4, A5
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V374000·2016-05-27
Land Rover Recalls Range Rovers Due to Air Bag Inflator Rupture Risk
Jaguar Land Rover is recalling 2007-2011 Range Rovers in specific US regions because passenger air bag inflators may rupture during deployment, potentially causing serious injury.
Product
LAND ROVER — LAND ROVER RANGE ROVER
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·16177·2016-05-26
Rheem Recalls Electric Water Heaters Due to Fire and Burn Hazards
Rheem is recalling about 54,000 Performance Platinum electric water heaters sold at Home Depot because the control panel can overheat, posing fire and burn risks.
Product
Rheem electric water heaters
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·16V366000·2016-05-26
Daimler Trucks Recalls 2015-2016 FCCC Trucks for Steering Defect
Daimler Trucks North America is recalling 2015-2016 FCCC trucks because a steering box defect could cause sudden loss of steering ability.
Product
FCCC — FCCC XBR, XCM, XCR, XBP
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V370000·2016-05-26
Ducati Recalls 2016 XDiavel S Motorcycles Due to Rear Wheel Installation Defect
Ducati is recalling 925 model year 2016 XDiavel S motorcycles because the rear wheel may be incorrectly installed, which could cause a loss of braking and power transmission, increasing crash risk.
Product
DUCATI — DUCATI XDIAVEL S
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V363000·2016-05-26
Mercedes-Benz Recalls Vehicles Due to Air Bag Inflator Rupture Risk
Mercedes-Benz is recalling specific 2008-2011 models because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
Product
MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ C300, C350, C63, GLK350
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V367000·2016-05-26
Toyota Recalls 2015 Yaris Vehicles Due to Front Strut Bearing Defect
Toyota is recalling 2015 Yaris vehicles because front strut mounting bearings can be damaged by high loads, potentially causing loss of vehicle stability and increasing crash risk.
Product
TOYOTA — TOYOTA YARIS
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1614-2016·2016-05-25
Monteris Medical Recalls NeuroBlate Laser Probes Due to Lens Fracture
Monteris Medical Corp is recalling 121 NeuroBlate System SideFire Select 2.2 mm Directional Laser Probes because a sapphire lens fractured during a procedure, introducing CO2 into a patient's brain.
Product
NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe, Sterile EO. Model #s SFS000-01,SFS002-01, SFS122-01, SFS222-01, SFS322-01, SFS422-01, and SFS522-01. NeuroBlate System SideFire Select Directional Laser Probes are part of the NeuroBlate System. The Monteris…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1332-2016·2016-05-25
Germinados Campo Verde Recalls Alfalfa Sprouts Linked to Salmonella
Germinados Campo Verde is recalling alfalfa sprouts from Puerto Rico due to a link to seed contaminated with Salmonella.
Product
Alfalfa Sprout Product***Germinados Campo Verde***San Sebastian, Puerto Rico
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1359-2016·2016-05-25
Sugarfina Chocolate Malt Balls Recalled for Undeclared Peanuts
Sugarfina, LLC is recalling Chocolate Malt Balls because they contain undeclared peanuts, a major food allergen.
Product
Sugarfina Chocolate Malt Balls UPC Code 840278113565 SKU K1159
Category
Food
Distribution
25 states
SevereNHTSA·16V359000·2016-05-25
Subaru and Saab Recall Vehicles for Air Bag Inflator Rupture Risk
Subaru is recalling specific 2003-2008 vehicles because passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.
Product
SUBARU — SUBARU, SAAB OUTBACK, BAJA, LEGACY, IMPREZA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V353000·2016-05-25
Rosenbauer Commander Recall: Air Suspension Seats May Separate in Collision
Rosenbauer is recalling 2012-2016 Commander vehicles because Battalion air suspension seats may separate from their base in a frontal collision, increasing injury risk.
Product
ROSENBAUER — ROSENBAUER COMMANDER
Category
Vehicle
Distribution
Distributed nationwide

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24401–24425 of 39708