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

30801–30825 of 39756

SevereFDA (Food)·F-2338-2014·2014-08-27
CaCoCo Superfood Drinking Chocolate Recalled for Potential Salmonella Contamination
CaCoCo, Inc. is recalling specific lots of Superfood Drinking Chocolate because an organic ingredient used in the product is under recall for potential Salmonella contamination.
Product
CaCoCo Superfood Drinking Chocolate; Original - Flavor Melody: Sweet, Playful, Perfectly Spiced Raw Chocolate. Gluten-free/Vegan/Raw Sold in 8 .14 oz (231 g). o and 2 lb. bags. Ingredients: Cacao Butter, Maca, Coconut Crystal Sugar,Carob, Cacao Bean, Cacao Powder, Lucuma…
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-1545-2014·2014-08-27
Fresenius Kabi Recalls Propranolol Hydrochloride Injection Due to API Deficiencies
Fresenius Kabi USA, LLC is recalling 56,060 vials of Propranolol Hydrochloride Injection because the active ingredient supplier received citations for critical manufacturing deficiencies.
Product
PROPRANOLOL — PROPRANOLOL (PROPRANOLOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1555-2014·2014-08-27
Healix Recalls Fentanyl Infusion Bags Due to Sterility Concerns
Healix Infusion Therapy is recalling compounded fentanyl infusion bags distributed in Texas and Georgia because the supplier recalled the source fentanyl due to loose or missing vial crimps.
Product
fentaNYL 5000 mcg/250 mL (20 mcg/mL) in 0.9% Sodium Chloride in a flexable bag, COMPOUNDED DRUG For Institutional or Office Use Only--Not for Resale, Federal Law Prohibits Dispensing without Prescription Healix Infusion Therapy, Inc. (866) 298-4826 1075 West Park One Drive…
Category
Drug
Distribution
2 states
SevereFDA (Drugs)·D-1547-2014·2014-08-27
Hospira Recalls Propofol Vials Due to Metallic Particulate Matter
Hospira Inc. is recalling 844,300 vials of Propofol Injectable Emulsion because glass defects allowed metallic particulates to enter the solution.
Product
PROPOFOL — PROPOFOL (PROPOFOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-2332-2014·2014-08-27
BrandStorm Recalls Organic Carob Powder Due to Salmonella Contamination Risk
BrandStorm Inc is recalling Organic Carob Powder because it may be contaminated with Salmonella. The affected product was distributed in North Dakota.
Product
Organic Carob Powder, Net Wt. 55lbs (25kg), Product Code: CAROB-100
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2256-2014·2014-08-27
Ortho Development Recalls Knee Implants Due to Improper Foil Pouch Sealing
Ortho Development is recalling various knee implant components because foil pouches failed to seal properly, allowing air to enter and potentially degrading the material properties of the implants.
Product
Tibila Insert UC, Balanced Knee System, REF163-3YYY Product Usage: UHMWPE component used in TKA procedures to serve as a tibial bearing surface for articulation with the femoral component
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-2335-2014·2014-08-27
Natural Grocers Recalls Organic Chunks of Energy Carob Supergreens for Salmonella Risk
Natural Grocers by Vitamin Cottage is recalling Organic Chunks of Energy Carob Supergreens due to the potential presence of Salmonella.
Product
Natural Grocers Organic Chunks of Energy Carob Supergreens, 0.70 lb. random weight, Packaged in Plastic Bags, Packaged by Vitamin Cottage Natural Food Markets, Inc. Lakewood, CO 80228 (303) 986-4600
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1549-2014·2014-08-27
Doctor's Best Red Yeast Rice Recalled for Undeclared Lovastatin
Doctor's Best is recalling Red Yeast Rice 1200 capsules because FDA analysis found undeclared lovastatin, making it an unapproved new drug.
Product
Doctor's Best Red Yeast Rice 1200, 600 mg Capsules, 120-count bottle. UPC 753950001183, Manufactured for Doctor's Best San Clemente, CA 92673
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·14262·2014-08-26
Hewlett-Packard Recalls Notebook Computer AC Power Cords Due to Fire and Burn Hazards
Hewlett-Packard is recalling specific AC power cords for notebook computers because they can overheat, posing a fire and burn hazard.
Product
Hewlett-Packard and Compaq notebook computer AC power cords
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·14E056000·2014-08-26
Agility Fuel Systems Recalls CNG Fuel Hoses Due to Corrosion Risk
Agility Fuel Systems is recalling specific CNG fuel systems because a hose component may corrode and leak gas, increasing fire risk.
Product
FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V517000·2014-08-26
NABI Transit Bus Recall for CNG Fuel Tank Abrasion Risk
NABI is recalling 2012-2014 31LFW and 40LFW transit buses because CNG fuel tanks may be abraded by pressure relief devices, increasing fire risk.
Product
NABI — NABI 40LFW, 31LFW
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V516000·2014-08-26
Audi Recalls 2013 Q7 Vehicles Due to Brake Booster Oil Leak Risk
Volkswagen is recalling 2013 Audi Q7 vehicles with 3.0L TDI engines because engine oil may leak into the brake booster, potentially causing a loss of power braking assist.
Product
AUDI — AUDI Q7
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·14261·2014-08-22
Ace Bayou Bean Bag Chairs Recalled Due to Suffocation and Choking Hazards
Ace Bayou is recalling about 2.2 million bean bag chairs because zippers can open, allowing children to crawl inside and suffocate or choke on foam beads.
Product
Bean bag chairs
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·14V514000·2014-08-22
Ford Recalls 2014 Focus and C-Max for Steering Gear Assembly Defect
Ford is recalling 2014 Focus and C-Max vehicles manufactured in August 2014 due to incorrectly assembled steering gears that may cause loss of steering control.
Product
FORD — FORD C-MAX, FOCUS
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·054-2014·2014-08-21
APPA Fine Foods Recalls Chicken Caesar Salad Kits for Listeria
APPA Fine Foods is recalling approximately 92,657 pounds of chicken Caesar salad kits due to possible Listeria monocytogenes contamination.
Product
California Firm Recalls Chicken Caesar Salad Kits For Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1535-2014·2014-08-20
Super ARTHGOLD Recalled for Undeclared Prescription Drugs
Super ARTHGOLD dietary supplement is being recalled because it contains undeclared prescription drugs and was marketed without FDA approval.
Product
Super ARTHGOLD 500mg, 120 Capsule Bottle, Dietary Supplement. Manufactured for & Distributed by Nanowellbeing Health, Inc., 14747 Artesia Blvd, #5V, La Mirada, CA 90638. UPC: 7 99475 35350 5.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1534-2014·2014-08-20
Lite Fit USA Recalled for Undeclared Sibutramine
Bacai, Inc. is voluntarily recalling Lite Fit USA supplements containing undeclared sibutramine, making them unapproved new drugs.
Product
Lite Fit USA, For Men & Women, Extreme Fat Burner, Suppresses Appetite, Boosts Metabolism, Limits Fat Absorption, Increases Energy, Prevents lipid formation by limiting fat absorption 30 pills /Bottle, Distributed by: Bacai, INC. www.litefitusa.com
Category
Drug
Distribution
0 states
SevereNHTSA·14E055000·2014-08-20
Thermo King Inverters Recalled for Fire Risk in Tractor Cabins
Thermo King is recalling specific 1100W, 1500W, and 2000W inverters sold between May and July 2014 because they may spark or overheat, posing a fire hazard.
Product
EQUIPMENT:ELECTRICAL recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2204-2014·2014-08-20
Gambro Recalls Prismaflex HF 1000 Dialysis Sets Due to Connector Breakage
Gambro Renal Products is recalling Prismaflex HF 1000 dialysis sets because connector breakages can cause leakage of liquid or blood.
Product
Prismaflex HF 1000. Product number 107140. Each set is packaged in a plastic pouch, 4 pouches per carton box
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2230-2014·2014-08-20
Zimmer Recalls 23.5 Degree Rasp Handle Assemblies Due to Assembly Failure
Zimmer, Inc. is recalling 412 units of 23.5 Degree Rasp Handle Assemblies because the handle may fail to remain assembled to the rasp during use.
Product
23.5 Deg Rasp Handle Assy- LEFT Nonsterile
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2225-2014·2014-08-20
Zimmer Recalls Nonsterile Orthopedic Rasp Handles Due to Assembly Failure
Zimmer, Inc. is recalling 412 nonsterile VER2 D8L Offset Rasp Handles because the handle may fail to remain assembled to the rasp during use.
Product
VER2 D8L OFFSET RASP HANDLE, RT Nonsterile
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-2313-2014·2014-08-20
Farmers Market Recalls Shelled Walnuts for Listeria Contamination Risk
Farmers Market is recalling 8 oz. packages of shelled walnuts due to potential Listeria monocytogenes contamination.
Product
Shelled walnuts, 8 oz., packed in a clear plastic container and sold under the Farmer's Market brand.
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-2177-2014·2014-08-20
Carestream Recalls Kodak DirectView DR 7500 X-Ray Systems Due to Loose Parts
Carestream Health is recalling 589 Kodak DirectView DR 7500 diagnostic x-ray systems because the x-ray tube assembly may detach from the overhead crane due to insufficiently tightened hardware.
Product
Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The DR 7500 system is a permanently installed diagnostic x-ray system composed of 4 main components: an operator console, over head tube crane, x-ray tube assembly including a collimator and stationary…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2135-2014·2014-08-20
Enhancement Medical Recalls Injectable Gel Due to Production Process Change
Enhancement Medical is recalling 17,875 units of EXP-150 Injectable Gel because a production change altered the final gel weight. The recall covers all lots distributed in the US and Canada.
Product
Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc Syringe with hyaluronic acid concentration of 20 mg/ml. Product Usage: Expression is labelled as an Intranasal Splint, intended to minimize bleeding and edema and to prevent adhesions between the septum…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2231-2014·2014-08-20
Zimmer Recalls 23.5 Degree Rasp Handle Assemblies Due to Assembly Failure
Zimmer, Inc. is recalling 23.5 Degree Rasp Handle Assemblies because the handle may fail to remain attached to the rasp during use.
Product
23.5 Deg Rasp Handle Assy- RIGHT Nonsterile
Category
Medical Device
Distribution
Distributed nationwide

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30801–30825 of 39756