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 deaths or serious injuries are reported, 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

10401–10425 of 36631

SevereFDA (Devices)·Z-0431-2021·2020-11-18
Stryker Recalls Cranial Perforators Due to Potential Metal Fragment Risk
Stryker is recalling Zyphr Disposable Cranial Perforators because a crack in the inner bit could release metal fragments into the surgical site or cause delayed disengagement.
Product
Stryker Zyphr Disposable Cranial Perforator, Large 14/11 mm- is a sterile, single use cutting accessory intended for cutting an 11 mm diameter access hole through the cranium of adult patients. Catalog Number: 5100-060-001
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0430-2021·2020-11-18
Stereotaxis Niobe ES System Recalled for Potential Fire Hazard
Stereotaxis Inc is recalling 121 Niobe ES Systems due to a potential fire risk in the internal computer cabinet.
Product
Niobe ES System, Models 001-006000-1 and 001-006100-1
Category
Medical Device
Distribution
0 states
SevereNHTSA·20V713000·2020-11-18
Lamborghini Recalls 2019-2020 Urus Vehicles Due to Fuel Line Fire Risk
Lamborghini is recalling 2,831 2019-2020 Urus vehicles because high engine temperatures may damage the fuel line connector, causing a leak and increasing fire risk.
Product
LAMBORGHINI — LAMBORGHINI URUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V709000·2020-11-17
Tesla Recalls 2020 Model Y Vehicles for Front Suspension Bolt Issue
Tesla is recalling 2020 Model Y vehicles because front upper control arm bolts may not be properly tightened, increasing crash risk.
Product
TESLA — TESLA MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20E085000·2020-11-17
Denso Recalls Fuel Pumps Due to Impeller Cracking and Engine Stalling Risk
Denso is recalling fuel pumps where an impeller may crack and deform, causing the pump to fail. This failure can cause the engine to stall while driving, increasing the risk of a crash.
Product
FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20E086000·2020-11-16
Aries Recalls Tow Hitches Due to Potential Structural Failure
Aries Industries is recalling certain Class 3 and Class 4 tow hitches because they may not support rated weights, risking hitch failure and vehicle separation.
Product
TRAILER HITCHES recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V702000·2020-11-13
2021 Volkswagen Atlas Tires Recalled for Over-Cure Defect
Volkswagen is recalling certain 2021 Atlas and 2020-2021 Atlas Cross Sport vehicles with potentially over-cured Continental Cross Contact LX Sport tires. Over-cured tires can cause sidewall breaks or tread separation, increasing crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V704000·2020-11-13
Zero Motorcycles Recalls 2020 SR/F and SR/S Models for Brake Switch Defect
Zero Motorcycles is recalling 2020 SR/F and SR/S motorcycles because water can enter the front brake switch, preventing the brake light from illuminating and increasing crash risk.
Product
ZERO — ZERO SR/F, SR/S
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V701000·2020-11-13
Chevrolet Bolt EV Recalled Due to High Voltage Battery Fire Risk
General Motors is recalling 2017-2019 Chevrolet Bolt EVs because the high voltage battery could catch fire when charged to full capacity, increasing the risk of injury.
Product
CHEVROLET — CHEVROLET BOLT EV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V697000·2020-11-12
Lion Electric Recalls 2016-2019 School Buses Due to Wheelchair Anchor Defect
Lion Electric is recalling 2016-2019 Lion C and 360 school buses with wheelchair lifts because shoulder belt and ground anchors may detach in a crash.
Product
LION — LION LIONC, 360
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·21708·2020-11-12
InvoSpa Recalls Electric Throw Heated Blankets Due to Fire and Burn Hazards
InvoSpa is recalling electric throw heated blankets sold on Amazon.com because they can overheat, posing fire and burn hazards.
Product
Electric Throw Heated Blankets
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·20V699000·2020-11-12
Jeep Grand Cherokee Recalled for EGR Cooler Fire Risk
Chrysler is recalling 2014-2019 Jeep Grand Cherokee vehicles with 3.0L EcoDiesel engines because a cracked EGR cooler may cause an intake manifold fire.
Product
JEEP — JEEP GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V696000·2020-11-11
Terex Recalls TL80 and TL100 Aerial Devices Due to Bolt Failure Risk
Terex is recalling 2019-2020 TL80 and TL100 aerial devices because rotation bearing bolts may loosen and fail, potentially causing the boom to fall.
Product
TEREX — TEREX TL100, TL80
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0399-2021·2020-11-11
Cook Inc. Recalls Fixed Core Wire Guides Due to Manufacturing Defects
Cook Inc. is recalling 61 Fixed Core Wire Guides that may be bent or contain loose foreign matter due to being dropped during manufacturing.
Product
Fixed Core Wire Guide, RPN TSCF-35-260-3, GPN G00517. The product is a curved wire guide with PTFE coating manufactured from stainless steel. To assist in inserting catheters, introducer sheaths, and other medical devices in vascular applications.
Category
Medical Device
Distribution
5 states
SevereFDA (Drugs)·D-0058-2021·2020-11-11
Direct Rx Recalls Metformin Hydrochloride Extended Release Due to NDMA Impurity
Direct Rx is recalling 88 bottles of Metformin Hydrochloride Extended Release 500 mg in Florida due to NDMA impurity levels above acceptable intake.
Product
METFORMIN HYDROCHLORIDE EXTENDED RELEASE — METFORMIN HYDROCHLORIDE EXTENDED RELEASE (METFORMIN HYDROCHLORIDE)
Category
Drug
Distribution
1 state
SevereFDA (Devices)·Z-0375-2021·2020-11-11
Zimmer Biomet Recalls Hip Prosthesis Components Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D. Cup with Spacers, 55 mm Number: 00-8065-652-22
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0330-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Hip Cups Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 acetabular hip cup components because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D. Cup with Spacers, 49 mm Item Number: 00-8065-546-26
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0060-2021·2020-11-11
PD-Rx Recalls Metformin Hydrochloride Extended Release Tablets Due to NDMA
PD-Rx Pharmaceuticals is recalling 125 bottles of Metformin Hydrochloride Extended Release tablets because of NDMA impurity levels above acceptable limits.
Product
METFORMIN HYDROCHLORIDE EXTENDED RELEASE — METFORMIN HYDROCHLORIDE EXTENDED RELEASE (METFORMIN HYDROCHLORIDE)
Category
Drug
Distribution
16 states
SevereFDA (Drugs)·D-0056-2021·2020-11-11
Denton Pharma Recalls Metformin Hydrochloride Tablets Due to NDMA Impurity
Denton Pharma, Inc. is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg due to the detection of N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels.
Product
Metformin Hydrochloride Extended-Release Tablets USP 750 mg, 30 Tablets bottle, Rx Only, Time-Cap Labs, Inc., Repackaged By: Northwind Pharmaceuticals North Blenheim NY 12131 NDC 70934-334-30
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0344-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Hip Prosthesis Cups Due to Sterilant Concerns
Zimmer Biomet is recalling 412 acetabular hip prosthesis cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Neutral, O.D. Cup with Spacers, 55 mm Item Number: 00-8065-552-32
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0333-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Hip Cup Components Due to Sterilant Concerns
Zimmer Biomet is recalling 412 acetabular hip cup components because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22mm, Neutral, O.D. Cup with Spacers, 51 mm Item Number: 00-8065-548-22
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0338-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Hip Cups Due to Sterilant Biocompatibility Concerns
Zimmer Biomet is recalling 412 acetabular hip cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D. Cup with Spacers, 53 mm Item Number: 00-8065-550-26
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0062-2021·2020-11-11
Metformin Hydrochloride Extended Release Tablets Recalled for NDMA Impurity
Marksans Pharma Limited is recalling Metformin Hydrochloride Extended Release tablets due to N-Nitrosodimethylamine (NDMA) impurity levels above acceptable intake limits.
Product
METFORMIN HYDROCHLORIDE EXTENDED RELEASE — METFORMIN HYDROCHLORIDE EXTENDED RELEASE (METFORMIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0335-2021·2020-11-11
Zimmer Biomet Recalls Acetabular Cup Hip Prosthesis Due to Sterilant Concerns
Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.
Product
ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, Neutral, O.D. Cup with Spacers, 51 mm Item Number: 00-8065-548-28
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0067-2021·2020-11-11
Nostrum Recalls Metformin Hydrochloride Extended-Release Tablets Due to NDMA Impurity
Nostrum Laboratories is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg because the NDMA impurity level exceeds acceptable intake limits.
Product
Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, 100 count bottles, Rx Only. Manufactured by: Nostrum Laboratories, Inc. Kansas City, MO 64120. NDC 29033-056-01
Category
Drug
Distribution
Distributed nationwide

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10401–10425 of 36631