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

33976–34000 of 39756

SevereFDA (Devices)·Z-2130-2013·2013-09-04
Stryker Triathlon Tibial Alignment Ankle Clamp Recalled for Cracks
Stryker is recalling 10,537 Triathlon Tibial Alignment Ankle Clamps due to cracks or fractures. The instruments are used in total knee arthroplasty.
Product
Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp extramedullary (EM) referencing instrument (Cat. No. 6541-2-609), for use in Total Knee Arthroplasty (TKA) when the surgeon elects to use Stryker's Triathlon Total Knee System in conjunction with EM referencing.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1853-2013·2013-09-04
See's Candies Recalls Dark Chocolate Blueberries Due to Missing Milk Labeling
See's Candies is recalling Dark Chocolate Blueberries because milk was omitted from the ingredient list. The product was distributed in the US, Hong Kong, and Taiwan.
Product
See's Candies, Van Doren Dark Chocolate Blueberries; 8 oz. clear plastic packages. See's Candies Inc./See's Candy Shops Inc: South San Francisco, CA 94080/Los Angeles, CA 90016
Category
Food
Distribution
0 states
SevereFDA (Food)·F-1851-2013·2013-09-04
Whole Foods Recalls Morbier Cheese Due to Listeria Risk
Whole Foods Market is recalling specific varieties of Trois Comtois Morbier cheese due to potential Listeria monocytogenes contamination linked to a French supplier recall.
Product
Trois Comtois Morbier Cheese labeled as follows: Morbier Raw Milk PLU 293358; Morbier AOC Le Trois PLU 293608; Morbier Raw Milk French Cheese PLU 293358; and Morbier Les Trois Comtois PLU 293608, Whole Foods Market
Category
Food
Distribution
15 states
SevereFDA (Food)·F-1857-2013·2013-09-04
Whole Foods Recalls Blueberry Crostata for Unlabeled Egg Allergen
Whole Foods Market is recalling Blueberry Crostata pies because egg wash is used in the product but is not listed on the ingredient or allergen statement.
Product
Blueberry Crostata, 1 pie Net. Wt. 1 lb. 6 oz (624 g) UPC: 0216733009993 Whole Foods Market Inc., Emeryville, CA 94608
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1850-2013·2013-09-04
Les 3 Comtois Recalls Morbier Cheese Due to Listeria
Les 3 Comtois is recalling 83 cases of Morbier cheese distributed in California, Illinois, and Wisconsin because FDA analysis detected Listeria monocytogenes.
Product
Morbier Les 3 Comtois, 11 lb. wheel; packaged in a cardboard case; one per case; refrigerated
Category
Food
Distribution
3 states
SevereCPSC·13275·2013-09-03
Target Recalls White Floor Lamps Due to Fire and Shock Hazard
Target is recalling approximately 25,000 white floor lamps sold in the U.S. and Canada due to a fire and shock hazard. Consumers should stop using the lamps and return them for a refund.
Product
White 2-Bulb Floor Lamp
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·13V392000·2013-08-30
Spartan Motor Home Chassis Recall for ABS Valve Fracture Risk
Spartan is recalling 2009-2014 motor home chassis because the ABS modulator valve may fracture, increasing stopping distance or causing the vehicle to pull.
Product
SPARTAN — SPARTAN K2, MM, K3
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·13V391000·2013-08-30
Indian Motorcycle Recalls 861 Models for Rear Rim Cracking Defect
Indian Motorcycle is recalling 861 motorcycles from 2009-2013 because the rear rim may crack, causing a flat tire and potential loss of control.
Product
INDIAN — INDIAN DARK HORSE, CHIEF STANDARD, BOMBER, ROADMASTER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·13V393000·2013-08-30
Dutchmen Voltage Recalled for Generator Fuel Filter Clamp Defect
Dutchmen is recalling 2014 Voltage recreational vehicles because the generator fuel filter clamp may be installed incorrectly. This defect could cause a fuel leak, increasing the risk of fire, injury, or property damage.
Product
DUTCHMEN — DUTCHMEN VOLTAGE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·13V385000·2013-08-29
Ford Recalls 2005-2011 Vehicles for Steering Column Corrosion Risk
Ford is recalling 2005-2011 Crown Victoria, Grand Marquis, and Town Car vehicles in specific states because severe corrosion can cause steering loss.
Product
MERCURY — MERCURY, FORD, LINCOLN GRAND MARQUIS, CROWN VICTORIA, TOWN CAR
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1828-2013·2013-08-28
NuGo Dark Mocha Non-Dairy Coffee Creamer Recalled for Undeclared Milk
NuGo Nutrition HQ is recalling Dark Mocha Non-Dairy coffee creamer because it may contain undeclared milk, posing a risk to people with milk allergies.
Product
NuGo Dark Mocha, 1.59 oz (45g) Non-Dairy
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1830-2013·2013-08-28
NuGo Dark Peanut Butter Cup Recalled for Undeclared Milk
NuGo Nutrition HQ is recalling Dark Peanut Butter Cups labeled as non-dairy because they may contain undeclared milk.
Product
NuGo Dark Peanut Butter Cup, 1.59 oz (45g) Non-Dairy
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1834-2013·2013-08-28
Whole Foods Recalls Crave Brothers Les Freres Cheese for Listeria Risk
Whole Foods Market is recalling Crave Brothers Les Freres cheese due to potential Listeria monocytogenes contamination, which can cause serious infections in vulnerable populations.
Product
Crave Brothers Les Freres cheese sold with labeling as: Les Freres, Crave Brothers Les Freres, Les Freres Wash Rind Product of USA, Crave Bros Les Freres, Crave Brothers Les Freres Cheese by Pound, Les Freres Crave Brothers, and Les Freres Crave Brothers PO-RK. Cheese was cut…
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1833-2013·2013-08-28
NuGo Slim Espresso Recalled for Undeclared Milk Allergen
NuGo Nutrition HQ is recalling NuGo Slim Espresso Non-Dairy products because they may contain undeclared milk. Consumers with milk allergies should not consume the product.
Product
NuGo Slim Espresso, 1.59 oz (45g) Non-Dairy
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1824-2013·2013-08-28
NuGo Free Dark Chocolate Trail Mix Bar Recalled for Undeclared Milk
NuGo Nutrition HQ is recalling specific lots of Free Dark Chocolate Trail Mix Bars because they may contain undeclared milk.
Product
NuGo Free Dark Chocolate Trail Mix Bar, 1.59 oz (45g) Non-Dairy
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1826-2013·2013-08-28
NuGo Free Carrot Cake Recalled for Undeclared Milk
NuGo Nutrition HQ is recalling NuGo Free Carrot Cake bars because they may contain undeclared milk, posing a risk to individuals with milk allergies.
Product
NuGo Free Carrot Cake, 1.59 oz (45g) Non-Dairy
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1827-2013·2013-08-28
NuGo Dark Chocolate Chocolate Chip Bars Recalled for Undeclared Milk
NuGo Nutrition HQ is recalling Dark Chocolate Chocolate Chip bars because they may contain undeclared milk, a major allergen.
Product
NuGo Dark Chocolate Chocolate Chip 1.59 oz (45g) Non-Dairy
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2028-2013·2013-08-28
Zimmer NexGen Knee Implant Components Recalled for Unapproved Combinations
Zimmer, Inc. is recalling NexGen Cruciate Retaining knee implant components because surgeons are using them in unapproved combinations.
Product
00595204110 Articular Surface XLPE CR ART SURF 5-6/STRGRN 10, Rx, Sterile; 00595204112 Articular Surface XLPE CR ART SURF 5-6/STRGRN 12, Rx, Sterile; 00595204114 Articular Surface XLPE CR ART SURF 5-6/STRGRN 14, Rx, Sterile; 00595204117 Articular Surface XLPE CR ART…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-915-2013·2013-08-28
Fresenius Kabi Recalls Irinotecan Hydrochloride Injection Due to Crystallization
Fresenius Kabi USA LLC is recalling 23,672 vials of Irinotecan Hydrochloride Injection because the active ingredient is precipitating in the solution.
Product
IRINOTECAN HYDROCHLORIDE INJECTION, 40 mg/2 mL (20 mg/mL), 2 mL Single Dose Vial, Rx only, Manufactured for: APP Pharmaceuticals, LLC, Schaumburg, IL 60173, NDC 63323-193-02, UPC 3 63323 19302 7.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·13V386000·2013-08-28
2013 Can-Am Spyder RT and ST Recalled for Brake Fire Risk
NHTSA is recalling 2013 Can-Am Spyder RT and ST motorcycles because a brake component may melt, causing fluid leaks that increase fire risk.
Product
CAN-AM — CAN-AM SPYDER RT, SPYDER ST
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1976-2013·2013-08-28
Stryker Oasys Midline Occiput Plate Recalled for Post-Operative Pin Fracture
Stryker Spine is recalling Oasys Midline Occiput Plates because customer reports indicate post-operative fracture of the pin connecting the tulip head to the plate body.
Product
Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large 4) Large Long 5) Mini. Allows for positioning directly on the midline keel of the occiput.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1832-2013·2013-08-28
NuGo Slim Crunchy Peanut Butter Recalled for Undeclared Milk
NuGo Nutrition HQ is recalling NuGo Slim Crunchy Peanut Butter bars because they may contain undeclared milk, a major food allergen.
Product
NuGo Slim Crunchy Peanut Butter, 1.59 oz (45g) Non-Dairy
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-912-2013·2013-08-28
Wise Woman Herbals Eyebright Eye Rinse Recalled for Sterility Concerns
Wise Woman Herbals is recalling Eyebright Concentrate Topical Eye Rinse because it was not manufactured under sterile conditions required for ophthalmic products.
Product
Eyebright Concentrate Topical Eye Rinse, 1, 2, 4, 8, 16 & 32 fl oz bottles, Produced and distributed by: Wise Woman Herbals, Creswell, OR
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2039-2013·2013-08-28
Zimmer Recalls NexGen Knee System Components Due to Unapproved Combinations
Zimmer, Inc. is recalling NexGen Cruciate Retaining Knee System components because surgeons are implanting unapproved combinations of micro and standard parts.
Product
00597502010 Provisional AC ART SURF PROV 12/PUR 10, Rx, Sterile; 00597502012 Provisional AC ART SURF PROV 12/PUR 12, Rx, Sterile; 00597502014 Provisional AC ART SURF PROV 12/PUR 14, Rx, Sterile; 00597502017 Provisional AC ART SURF PROV 12/PUR 17, Rx, Sterile…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2042-2013·2013-08-28
Zimmer NexGen Knee System Recalled for Unapproved Component Combinations
Zimmer, Inc. is recalling NexGen Cruciate Retaining Knee System components because surgeons are implanting unapproved combinations of micro and standard parts.
Product
00597102010 Provisional CR ART SURF PROV 12/PURPLE 10, Rx, Sterile; 00597102012 Provisional CR ART SURF PROV 12/PURPLE 12, Rx, Sterile; 00597102014 Provisional CR ART SURF PROV 12/PURPLE 14, Rx, Sterile; 00597102017 Provisional CR ART SURF PROV 12/PURPLE 17, Rx…
Category
Medical Device
Distribution
Distributed nationwide

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