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

25201–25225 of 26084

HighCPSC·21768·2021-07-27
Oculus Quest 2 Removable Foam Facial Interfaces Due to Skin Irritation Risk
Facebook Technologies is recalling about 4 million removable foam facial interfaces for Oculus Quest 2 virtual reality headsets because the foam can cause facial skin irritation and reactions. Consumers should stop using affected interfaces and contact the manufacturer for a free silicone replacement.
Product
Removable Foam Facial Interfaces for Oculus Quest 2 Virtual Reality Headsets
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V569000·2021-07-26
2021 Audi E-Tron recalled for brake booster defect
Volkswagen is recalling certain 2021 Audi E-Tron models due to improperly welded brake boosters that may separate, reducing braking assistance and stability control.
Product
AUDI — 2021 AUDI E-TRON
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V566000·2021-07-26
2021–2022 Spartan K2 RV Chassis Fuel Leak Recall
Shyft Group is recalling certain 2021–2022 Spartan K2 RV Chassis vehicles with Cummins L9 Diesel Engines due to fuel leaks from pressurized hoses. The leak may increase fire risk if an ignition source is present.
Product
SPARTAN — 2021 SPARTAN K2
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·21764·2021-07-22
Bel Furniture Recalls Barrington 5-Drawer Chests for Tip-Over Hazards
Bel Furniture is recalling about 90 Barrington 5-Drawer Chests because the dressers can tip over and trap children if not anchored to the wall. One child has already been injured when a chest tipped over.
Product
Barrington 5-Drawer Chests
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·21765·2021-07-22
Polaris GENERAL Recreational Off-Highway Vehicles Crash Hazard Recall
Polaris is recalling Model Year 2021 GENERAL 1000, GENERAL 4 1000, GENERAL XP 1000, and GENERAL XP 4 1000 recreational off-highway vehicles because a weld between the brake pedal pivot bracket and EPS mounting bracket can separate, resulting in loss of brake function.
Product
Model Year 2021 GENERAL 1000, GENERAL 4 1000, GENERAL XP 1000 and GENERAL XP 4 1000 ROVs
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V557000·2021-07-22
2021 Heartland Mallard Recreational Trailers Recalled for Refrigerator Vent Defect
Heartland is recalling certain 2021 Mallard and North Trail recreational trailers with improperly routed refrigerator roof vents. The defect risks fire and carbon monoxide poisoning.
Product
HEARTLAND — 2021 HEARTLAND MALLARD
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21766·2021-07-22
Polaris RZR Off-Road Vehicles Recalled for Fire Hazard
Polaris is recalling about 1,700 Model Year 2021 RZR Pro XP and RZR Pro XP 4 recreational off-road vehicles because a raised edge on the turbocharger casting can cause an oil leak and fire hazard.
Product
Model Year 2021 RZR Pro XP and RZR Pro XP 4 Recreational Off-Road Vehicles (ROVs)
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21767·2021-07-22
Can-Am Defender HD10 Side-by-Side Vehicles Recalled for Fire Hazard
BRP is recalling about 34,400 model years 2020 and 2021 Can-Am Defender HD10 side-by-side vehicles because the CVT air intake can become obstructed with snow, causing the drive belt to overheat and break and creating a fire hazard. BRP has received three reports of fires but no injuries.
Product
Model Years 2020 and 2021 Can-AM Defender HD10 side-by-side vehicles
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0694-2021·2021-07-21
Prairie Wolf Distillery Hand Sanitizer Recalled for Misleading Beverage-Like Packaging
Prairie Wolf Distillery Alcohol Antiseptic 80% hand sanitizer is being recalled because the bottles resemble beverage containers, creating a risk of accidental ingestion. The recall affects all lots of both the 500 mL and 591 mL sizes distributed nationwide.
Product
Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer, packaged in a) (16.9oz) 500 mL (UPC 8 60003 31899 7, NDC: 73891-100-14); and b) (20oz) 591 mL (UPC 8 60003 65984 7 NDC: 73891-100-15) bottles, Prairie Wolf Distillery, Guthrie, Oklahoma
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1974-2021·2021-07-21
Philips Respironics ventilators recalled for degrading foam and chemical hazards
Philips Respironics ventilators are recalled because foam components may degrade and release particles and chemicals that patients could inhale.
Product
SystemOne (Q-Series), DreamStation, DreamStation Go, Dorma 400, Dorma 500, REMstar SE Auto Noncontinuous Ventilators The Philips Respironics E30 ventilator is intended to provide invasive and non-invasive ventilatory support for individuals with Respiratory Insufficiency. It
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2019-2021·2021-07-21
INTUA CRT-P Pacemakers Recalled Due to Battery Degradation Risk
The INTUA CRT-P pacemakers (1,707 units) may develop high internal battery impedance later in device life, causing system resets and triggering Safety Mode. Therapy continues but device replacement is required.
Product
INTUA CRT-P, Model Numbers: a) V272 b) V273 c) W273
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2018-2021·2021-07-21
Boston Scientific INGENIO CRT-P Pacemakers Recalled for Battery Defect
Boston Scientific is recalling INGENIO CRT-P pacemakers that may develop high internal battery impedance, causing unexpected device resets and Safety Mode activation. Affected devices require replacement.
Product
INVIVE CRT-P, Model Numbers: a) V172 b) V173 c) V182 d) V183 e) W172 f) W173
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1958-2021·2021-07-21
Philips BiPAP A-Series Ventilators Recalled for Foam Degradation Risk
Philips Respironics recalled 72,665 BiPAP A-Series ventilators worldwide. The foam in these devices may degrade into particles that could be inhaled or ingested, and may release chemicals.
Product
A-Series BiPAP A 40, A-Series BiPAP A30 Continuous Ventilator, Non-life Supporting
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2015-2021·2021-07-21
Boston Scientific ADVANTIO DR EL Pacemakers Recalled for Battery Malfunction
Boston Scientific is recalling ADVANTIO DR EL dual chamber pacemakers and CRT-Ps due to a latent battery condition that may cause system resets and trigger Safety Mode, requiring device replacement.
Product
ADVANTIO DR EL (pacemaker), Model Numbers: a) J064 b) J067 c) K064 (added 7/15/2021) d) K084 (added 7/15/2021) e) K087 (added 7/15/2021)
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2020-2021·2021-07-21
Boston Scientific INLIVEN CRT-P Pacemakers Battery Impedance Recall
Boston Scientific recalls dual chamber INGENIO family pacemakers and CRT-Ps with Extended Life batteries that may develop high internal impedance, causing Safety Mode and system resets, requiring device replacement.
Product
INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2017-2021·2021-07-21
VITALIO DR EL Pacemakers Recalled Due to Battery-Related Device Resets
Boston Scientific is recalling VITALIO DR EL pacemakers with Extended Life batteries due to a latent battery condition that may cause unexpected device resets and Safety Mode activation later in device life.
Product
VITALIO DR EL (pacemaker), Model Numbers: a) J274 b) J277 c) K274 (added 7/15/2021) d) K277 (added 7/15/2021) e) K284 (added 7/15/2021) f) K287 (added 7/15/2021)
Category
Medical Device
Distribution
0 states
SevereCPSC·21168·2021-07-21
Harbor Freight Tank Top Propane Heaters Recalled for Burn Hazard
Harbor Freight Tools is recalling about 350,000 One Stop Gardens tank top propane heaters because wind can redirect the flame to melt the safety shutoff, preventing the heater from turning off if tipped. Three minor burn injuries have been reported.
Product
One Stop Gardens 15,000 and 30,000 BTU Tank Top Propane Heaters
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0657-2021·2021-07-21
Durisan Hand Sanitizing Wipes Recalled for Microbial Contamination
Sanit Technologies is recalling Durisan Antimicrobial Solutions Hand Sanitizing Wipes because certain lots were found to contain Burkholderia contaminans and/or yeast and mold through internal testing.
Product
Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizing Wipes, 0.13%, 160-count canister; Sanit Technologies, LLC, 7810 25th Court East, Sarasota, Florida 34243, UPC 8 52379 00631 8.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2016-2021·2021-07-21
INGENIO DR EL Pacemakers Recalled: Defective Battery May Trigger Safety Mode
Dual chamber INGENIO DR EL pacemakers with Extended Life batteries may develop high internal impedance, causing devices to enter Safety Mode later in life. Affected patients should contact their healthcare provider about replacement.
Product
INGENIO DR EL (pacemakers), Model Numbers: a) J174 b) J177 c) K174 (added 7/15/2021) d) K184 (added 7/15/2021) e) K187 (added 7/15/2021)
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1972-2021·2021-07-21
Philips Respironics E30 ventilator foam degradation poses inhalation hazard
Philips Respironics E30 ventilators may have polyurethane foam that degrades into particles. These particles can enter the air pathway and be inhaled or ingested by patients, or the foam may off-gas chemicals.
Product
Philips Respironics E30 with Humidifier, Continuous Ventilator, Minimum Ventilatory Support, Facility Use; Product Numbers DSX9999H11, INX9999H19, RINX9999H19 The Philips Respironics E30 ventilator is intended to provide invasive and non-invasive ventilatory support for indiv
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1973-2021·2021-07-21
Philips Respironics ventilators recalled due to foam degradation and chemical release
Philips Respironics ventilators and respiratory support devices are being recalled because polyurethane foam components may degrade into particles that can be inhaled or ingested, and the foam may release harmful chemicals.
Product
DreamStation ASV, DreamStation ST, AVAPS, SystemOne ASV4, C-Series ASV, C-Series S/T and AVAPS, OmniLab Advanced+ Continuous Ventilator, Non-life Supporting The Philips Respironics E30 ventilator is intended to provide invasive and non-invasive ventilatory support for individu
Category
Medical Device
Distribution
0 states
SevereFDA (Drugs)·D-0656-2021·2021-07-21
Durisan Antimicrobial Hand Sanitizer recalled for microbial contamination
Sanit Technologies is recalling Durisan Antimicrobial Solutions hand sanitizer due to internal testing that found contamination with Burkholderia contaminans and/or yeast and mold in certain lots.
Product
Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizer, listed as 0.1% or 0.13%, Alcohol-Free, packaged in a) 18 mL Net Content 0.61 fl oz credit card size container, (UPC 8 52379 00614 1); b) 50 mL Net Content 1.69 oz bottle, (UPC 8 52379 00634 9 and 8 52379 0061
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0774-2021·2021-07-21
Cooked Snow Crab Sections Recalled for Salmonella and Listeria
Cooked frozen snow crab sections from Crustaces Baie-Trinite Inc. are being recalled due to potential contamination with Salmonella and Listeria monocytogenes. The affected product was distributed to restaurant distributors in Massachusetts and Missouri.
Product
Cooked Snow Crab, Brine Frozen Sections, 2L and L sizes, Net Wt 13.15 kg / 29 lb
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-1956-2021·2021-07-21
Philips Respironics Continuous Ventilators Recalled for Foam Degradation Risk
Philips Respironics is recalling approximately 255,810 continuous ventilators because polyurethane foam may degrade into particles that could be inhaled or ingested, or release chemicals.
Product
Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0654-2021·2021-07-21
Poseidon Platinum 3500 Capsules Recalled for Undeclared Prescription Drugs
Poseidon Platinum 3500 capsules are being recalled because they contain undeclared sildenafil and tadalafil, which are prescription drugs that were not approved for this product. The safety and efficacy of these undeclared ingredients have not been established.
Product
Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
Category
Drug
Distribution
0 states

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25201–25225 of 26084