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

22001–22025 of 25981

HighFDA (Drugs)·D-0757-2022·2022-04-13
Accuretic Blood Pressure Tablets Recalled for Excess Chemical Impurity
Pfizer is recalling Accuretic blood pressure tablets due to manufacturing deviations that resulted in N-nitroso chemical impurities exceeding safe intake limits. Patients should contact their pharmacist or physician.
Product
Accuretic (quinapril HCl/hydrochlorothiazide) Tablets, 20 mg/25 mg, 90 tablets bottles, Rx Only, Distributed by: Parke-Davis, Division of Pfizer Inc, NY, NY 10017, Made in Germany, NDC 0071-0223-23.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0892-2022·2022-04-13
Unauthorized SARS-CoV-2 Antigen Tests recalled for lack of FDA clearance
WHPM Inc. is recalling approximately 535,755 First SIGN SARS-CoV-2 Antigen Tests distributed in California, Florida, Louisiana, Massachusetts, and Texas. The tests were sold without FDA Emergency Use Authorization or clearance.
Product
First SIGN SARS-CoV-2 Antigen Test
Category
Medical Device
Distribution
5 states
HighFDA (Devices)·Z-0881-2022·2022-04-13
Philips HeartStart HS1 AED Pads: Potential Gel Separation Defect
Philips is recalling adult Smart PADS cartridges for HeartStart HS1 defibrillators due to potential gel separation from the pad backing. Affected pads may have reduced gel contact, potentially affecting device performance.
Product
Philips, REF M5071A, Adult. Smart PADS CARTRIDGE, 8+ years FOR USE WITH HEARSTART HS1 DEFIBRILLATORS
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V235000·2022-04-12
Tesla Model S Boombox function obscures pedestrian warning system sounds
Tesla is recalling certain 2020-2022 Model S, X, Y and 2017-2022 Model 3 vehicles. The Boombox feature can obscure Pedestrian Warning System sounds while driving. A free software update will disable Boombox in Drive, Neutral, and Reverse modes.
Product
TESLA — 2021 TESLA MODEL S
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V234000·2022-04-11
Newmar RVs recalled for unsecured seat wiring fire risk
Newmar is recalling multiple 2019–2022 RV models due to unsecured wiring beneath seats that can cause electrical short circuits and fire. Owners should contact their dealer for free inspection and repair.
Product
NEWMAR — 2019 NEWMAR BAY STAR SPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V233000·2022-04-08
2021-2022 Tesla Model X Side Curtain Air Bag Deployment Defect
Tesla is recalling certain 2021-2022 Model X vehicles due to a defect in the left or right front-row side curtain air bags that may not deploy properly when windows are lowered. Improper deployment increases the risk of injury during crashes.
Product
TESLA — 2021 TESLA MODEL X
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V230000·2022-04-08
Western Star trucks recalled for failing windshield wiper linkages
Daimler Trucks North America is recalling certain 2020-2022 Western Star 49X and 2021 Western Star 47X vehicles because windshield wiper linkages may break, causing wipers to fail and reducing visibility.
Product
WESTERN STAR — 2020 WESTERN STAR 49X
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V232000·2022-04-08
Mercedes-Benz 2018-2021 models recalled for rearview camera display failure
Mercedes-Benz is recalling 126,443 vehicles from 2018-2021 because the rearview camera display may fail to show the rear view due to a software error, reducing visibility and increasing crash risk.
Product
MERCEDES-BENZ — 2021 MERCEDES-BENZ AMG GLB35
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·22739·2022-04-07
Bestar Wall Beds Recalled Due to Detachment and Crush Hazards
Bestar wall beds can detach from the wall and fall, creating impact and crush hazards. One death and 60 additional injuries have been reported.
Product
Bestar Wall Beds
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·22738·2022-04-07
biOrigins Sodium Hydroxide Products Recalled for Non-Child-Resistant Packaging
CPSC recalls biOrigins sodium hydroxide products sold on Amazon from July 2020 through July 2021 due to non-child-resistant packaging and missing hazard label information. The product poses risk of chemical burns and skin/eye irritation to children.
Product
biOrigins Sodium Hydroxide Products
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V227000·2022-04-07
Western Star commercial trucks recalled for detaching hood air intake covers
Daimler Trucks North America is recalling certain 2020-2023 Western Star trucks equipped with side air intakes on the hood. The stainless steel cover may loosen and detach, creating a road hazard and increasing crash risk.
Product
WESTERN STAR — 2020 WESTERN STAR 49X
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0959-2022·2022-04-06
Cavendish Farms Frozen Hash Brown Patties Recalled for Undeclared Wheat and Barley
Cavendish Farms is recalling Les Fermes Frozen Hash Brown Potato Patties because they contain undeclared wheat and barley flour. People with allergies to wheat or barley should not consume the product.
Product
Les Fermes Cavendish Farms Frozen Original Hash Brown Potato Patties Net Wt, 42.3 (1.2 kg). 12 retail packages per case, 20 patties per retail tray pack. UPC: 0 56210 34217 1
Category
Food
Distribution
9 states
SevereFDA (Drugs)·D-0767-2022·2022-04-06
Meclizine Hydrochloride Tablets Recalled Due to Incorrect Label Mix-up
Jubilant Cadista Pharmaceuticals recalls Meclizine Hydrochloride Tablets with incorrect labeling. Bottles labeled as PredniSONE contain Meclizine, risking medication errors.
Product
MECLIZINE HYDROCHLORIDE — MECLIZINE HYDROCHLORIDE (MECLIZINE HYDROCLORIDE)
Category
Drug
Distribution
0 states
SevereFDA (Food)·F-0912-2022·2022-04-06
St. Benoit Yogurt Recalled for Undeclared Egg Allergen
St. Benoit French Vanilla Yogurt is being recalled because it contains undeclared egg, a common allergen. Consumers with egg allergies should not consume the product.
Product
St. Benoit French Vanilla Yogurt; from pasture raised Jersey cows. Packaged in glass jar, net wt. 4.75 oz., UPC 6 49241 92910 9, St. Benoit Creamery. Sonoma, CA 95476 Certified Organic by CCOF
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0913-2022·2022-04-06
Taiwan Best Quality Enoki Mushrooms Recalled for Listeria monocytogenes Contamination
Jan Fruits, Inc. is recalling Taiwan Best Quality Enoki Mushrooms (UPC 8 51084 00835 8) due to detection of Listeria monocytogenes. The product was distributed in California.
Product
Taiwan Best Quality Enoki Mushrooms; 200g/7.05 oz. clear plastic bag (50 bags/pcs per box). Product is in a clear bag with green bottom. UPC 8 51084 00835 8. Product of Taiwan Manufacturer: Changhua County Mushrooms Production Cooperative.
Category
Food
Distribution
1 state
SevereFDA (Food)·F-0910-2022·2022-04-06
Yogurt-Covered Raisins Recalled Nationwide Due to Undeclared Peanuts
Multiple brands of yogurt-covered raisins distributed nationwide are being recalled due to undeclared peanuts. Consumers with peanut allergies face a serious health risk.
Product
Woody's Smokehouse brand Yogurt Raisins, 12.3 oz. (348g), clear plastic bag with front and back labels, UPC 0 95248 65531 0. Packed especially for Woody's Smokehouse Inc., Centerville, TX 75833, 903-536-9663, Woody's-Smokehouse.com Texas Best Smokehouse brand Yogurt Raisins, 8 o
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0729-2022·2022-04-06
Gonadorelin injectable recalled for lack of sterility assurance
Drug Depot recalls 1,843 vials of Gonadorelin injectable nationwide due to lack of sterility assurance. Patients should consult their healthcare provider regarding previously dispensed doses.
Product
(CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0843-2022·2022-04-06
Hip prosthetic femoral head component size and offset labeling mismatch
Howmedica Osteonics is recalling 40 units of Biolox delta Ceramic V40 Femoral Head components where the size and/or offset may not match package labeling.
Product
Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0855-2022·2022-04-06
Medtronic MiniMed insulin pumps may not deliver basal insulin without configuration
Medtronic MiniMed insulin pumps may be used without programmed basal rates, causing insulin under-delivery and potentially severe high blood sugar. Patients must configure and save basal settings before use, but labeling doesn't clearly explain this requirement.
Product
MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782; MiniMed 770G: MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892; MiniMed 620G (OUS Only): MMT-1750; MiniMed 640G (OUS O
Category
Medical Device
Distribution
53 states
HighFDA (Food)·F-0909-2022·2022-04-06
Schwan's Spinach & Artichoke Dip recalled due to product mislabeling
Fairmont Foods is recalling Schwan's Spinach & Artichoke Dip because cartons may contain Chicken & Broccoli instead, creating potential allergen risks.
Product
Schwan's Spinach & Artichoke Dip. Item Number 061353, UPC 10038-68192. Net Wt. 24 oz. (1 lb. 8 oz.) 680g. Contains: 2 Bowls. Keep Frozen. Cook Thoroughly. Spinach and Artichokes blended with cream cheese and sour cream with Parmesan, Mozzarella, and Romano Cheeses. Dist
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0854-2022·2022-04-06
Illumina NextSeq 550Dx DNA Analyzer Recalled for Short Circuit Risk
Illumina is recalling 674 NextSeq 550Dx DNA sequence analyzers worldwide. A short circuit may occur after reconnecting circuit components, causing the device to become inoperable.
Product
Illumina NextSeq 550Dx, REF: 20005715, CE, IVD
Category
Medical Device
Distribution
31 states
HighFDA (Drugs)·D-0737-2022·2022-04-06
Lansoprazole Capsules Recalled for Failed Dissolution in Stability Testing
Dr. Reddy's Laboratories is recalling specific lots of Lansoprazole 15 mg delayed-release capsules nationwide because the capsules failed to dissolve properly during long-term stability testing, which could affect medication effectiveness.
Product
LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0850-2022·2022-04-06
Medical software recall: RayStation radiation therapy dose calculation errors
RayStation and RayPlan radiation therapy planning software may calculate incorrect radiation doses due to a source-to-skin distance calculation error. The FDA Class II recall affects 149 units distributed in the US.
Product
RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5 Service Pack 2 (5.0.2.35), RayStation 5 Service Pack 3 (5.0.3.17), RayStation 6/RayPlan 2 (6.0.0.24), RayStation 6/RayPlan 2 Service Pack 1 (6.1.1.2), RayS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0848-2022·2022-04-06
Radiation therapy planning software subject to jaw positioning errors during optimization
RayStation radiation therapy planning software (versions 6-11A) may unexpectedly change jaw positions during optimization after dose or target modifications. Users should verify treatment plans carefully before delivery.
Product
TomoHelical and TomoDirect plans in RayStation 6, 7, 8A, 8B, 9A, 9B, 10A, 10B and 11A. Build Numbers: 6.1.1.2, 6.2.0.7, 6.3.0.6, 7.0.0.19, 8.0.0.61, 8.0.1.10, 8.1.0.47, 8.1.1.8, 8.1.2.5, 9.0.0.113, 9.1.0.933, 9.2.0.483, 10.0.0.1154, 10.0.1.52, 10.1.0.613, 11.0.0.951 or 11.0.1.2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0852-2022·2022-04-06
Hanger-Bar 2P 45cm Recalled for Fall Hazard from Loosened Set Screw
Human Care USA, Inc. is recalling the Hanger-Bar 2P 45cm because the set screw may loosen due to a manufacturing defect, creating a fall hazard.
Product
Hanger-Bar 2P 45cm
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

22001–22025 of 25981