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

16051–16075 of 31567

ModerateFDA (Devices)·Z-0617-2024·2024-01-03
Medivators Advantage Endoscope Hookup Accessories Recalled for Illegible Identification Labels
Steris Corporation recalls Medivators Advantage endoscope hookup accessories because identification labels become illegible as ink degrades, potentially preventing proper hookup identification and delaying patient procedures.
Product
Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS Pass Thru Automated Endoscope Reprocessors Model # Model Description 2-8-001 HU ZERO CHANNEL NO LT 2-8-010 ASSY, HOOK-UP, OLYMPUS 2-8-014 HOOKUP, OPTIM LT 2-8-030 ASSY, HOOKUP, PENTAX-0K 2-8-040 AS
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0195-2024·2024-01-03
OTC Throat Lozenges Recalled for Temperature Storage Deviation
Ricola Cherry Honey Herb Throat Drops are recalled because products in batch 2000058693 were exposed to temperatures outside the labeled storage conditions during distribution. The Class II recall affects nationwide shipments.
Product
NATURAL CHERRY HONEY HERB THROAT DROPS — NATURAL CHERRY HONEY HERB THROAT DROPS (MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0178-2024·2024-01-03
Doxycycline Capsules Recalled Due to Temperature Storage Deviation
Cardinal Healthcare is recalling Doxycycline 100 mg Capsules nationwide due to exposure to temperatures outside labeled storage conditions. No illnesses have been reported.
Product
DOXYCYCLINE — DOXYCYCLINE (DOXYCYCLINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0187-2024·2024-01-03
Birth control tablets recalled nationwide for temperature storage deviation
Lillow oral contraceptive tablets (batch A5921) have been recalled nationwide by Cardinal Healthcare due to exposure to temperatures outside labeled storage conditions.
Product
Lillow (Levonorgestrel and Ethinyl Estradiol Tablets, USP), 0.15 mg/0.03 mg, 1 Blister Pack Containing 28 Tablets, Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC 69238-1554-6
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0194-2024·2024-01-03
Propranolol Hydrochloride 20 mg Tablets Recalled for Temperature Storage Deviations
Propranolol Hydrochloride tablets have been recalled nationwide. Products were exposed to temperatures outside labeled storage conditions during manufacturing, potentially affecting drug stability.
Product
PROPRANOLOL HYDROCHLORIDE — PROPRANOLOL HYDROCHLORIDE (PROPRANOLOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0183-2024·2024-01-03
Folic Acid tablets recalled for improper storage conditions
Cardinal Healthcare recalls Folic Acid tablets (1mg, batch H08221) nationwide due to storage temperature deviations during manufacturing. No illnesses reported.
Product
FOLIC ACID — FOLIC ACID (FOLIC ACID)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0185-2024·2024-01-03
FDA Recalls Jardiance Diabetes Tablets Due to Storage Temperature Deviations
Jardiance 25 mg tablets distributed nationwide were recalled due to CGMP deviations where products were exposed to temperatures outside the labeled storage conditions. The recall affects batch D41919.
Product
JARDIANCE — JARDIANCE (EMPAGLIFLOZIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0172-2024·2024-01-03
Chlorthalidone Tablets Recalled for Temperature Storage Deviations
Cardinal Healthcare is recalling Chlorthalidone Tablets, 25mg (Batch 2107329UM) distributed nationwide because products were exposed to temperatures outside the labeled storage conditions.
Product
CHLORTHALIDONE — CHLORTHALIDONE (CHLORTHALIDONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0160-2024·2024-01-03
Anoro Ellipta inhalation powder recalled for failed release testing defect
GlaxoSmithKline is recalling 67,508 Anoro Ellipta inhalers nationwide because coarse particle mass failed release testing and was found out of specification. No illnesses have been reported.
Product
ANORO ELLIPTA — ANORO ELLIPTA (UMECLIDINIUM BROMIDE AND VILANTEROL TRIFENATATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0168-2024·2024-01-03
Prescription thyroid drug recalled due to temperature storage deviation
ARMOUR THYROID 120 mg tablets in batch W05543 are being recalled nationwide due to exposure to temperatures outside the labeled storage conditions. No illnesses or injuries have been reported.
Product
ARMOUR THYROID — ARMOUR THYROID (THYROID, PORCINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0662-2024·2024-01-03
Bowl & Basket Zero Calorie Sweetener recalled for undeclared aspartame
Wakefern Foods Corp. is recalling Bowl & Basket Zero Calorie with Sucralose Sweetener due to undeclared aspartame and missing phenylalanine warning. The product poses a risk to consumers with phenylketonuria (PKU).
Product
Bowl & Basket Zero Calorie with Sucralose Sweetener 100 count, UPC 0-41190-06855-5, 12 retail cartons per wholesale case
Category
Food
Distribution
9 states
ModerateFDA (Drugs)·D-0174-2024·2024-01-03
Colgate Total SF Toothpaste recalled for improper storage temperature exposure
Colgate Total SF Toothpaste (Batch 1293US561C, 4.8 oz, Clean Mint) distributed nationwide is being recalled due to CGMP deviations where products were exposed to temperatures outside labeled storage conditions.
Product
Colgate Total SF Toothpaste, Net Wt 4.8 oz (136 g), Stannous Fluoride 0.454%, Clean Mint, Dist. by: COLGATE-PALMOLIVE CO., New York, NY 10022 USA
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0186-2024·2024-01-03
Leader Nasal Decongestant PE recalled due to improper storage conditions
Cardinal Healthcare is recalling Leader Nasal Decongestant PE (Phenylephrine HCl 10 mg, 18-tablet cartons) nationwide because products were exposed to temperatures outside the labeled storage conditions. Batch P125514 is affected.
Product
Leader Nasal Decongestant PE (Phenylephrine HCl 10 mg), 18 Tablets per cartons, Distributed By Cardinal Health, Dublin, Ohio 43017. NDC: 70000-0126-1
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0164-2024·2024-01-03
Allopurinol tablets recalled due to improper storage conditions
Cardinal Healthcare is recalling Allopurinol 300 MG tablets (batch L100813) nationwide because products were exposed to temperatures outside their labeled storage conditions. Patients should consult their healthcare provider.
Product
ALLOPURINOL — ALLOPURINOL (ALLOPURINOL)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24V060000·2024-01-02
General Motors Recalls Pickup Trucks with Defective Power Tailgate Latches
General Motors is recalling certain 2020-2024 Chevrolet Silverado and GMC Sierra pickup trucks due to faulty electronic tailgate switches that may inadvertently unlatch while the vehicle is parked. The defect can allow the tailgate to open while driving, potentially causing cargo loss and creating a road hazard.
Product
CHEVROLET — 2020 CHEVROLET SILVERADO 2500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V061000·2024-01-02
Motorhome Seat Pedestal Weld Defect Causes Unsafe Seat Separation Risk
Jayco is recalling certain 2020-2023 Entegra motorhomes because passenger seats may have improperly welded pedestals that can separate and cause the seat to loosen or detach.
Product
ENTEGRA — 2022 ENTEGRA CORNERSTONE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V064000·2024-01-02
Multiple Honda and Acura models recalled for defective airbag sensor
Honda and Acura are recalling 750,114 vehicles from 2020-2022 model years. A defective front passenger seat weight sensor may fail to suppress the airbag, increasing the risk of injury in a crash.
Product
HONDA — 2022 HONDA CIVIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V078000·2024-01-02
Proterra Catalyst and ZX5 buses recalled for wiper motor failure
Proterra is recalling certain 2020–2022 Catalyst and ZX5 buses due to windshield wiper motor failure. Inoperative wipers reduce visibility and increase crash risk.
Product
PROTERRA — 2022 PROTERRA CATALYST
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V062000·2024-01-02
Tiffin Allegro Bay motorhomes recalled for battery fire risk
Tiffin is recalling certain 2022–2024 Allegro Bay motorhomes because batteries may shift during travel, causing electrical arcing and fire risk. Dealers will install new hold-down hardware at no charge.
Product
TIFFIN — 2022 TIFFIN ALLEGRO BAY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V065000·2024-01-02
2023 Hyundai IONIQ 5 and IONIQ 6 driveshaft replacement recall
Hyundai is recalling 2023 IONIQ 5, IONIQ 6, and Genesis GV60 vehicles for rear driveshafts that may break under load due to improper heat treatment, causing loss of drive power. Dealers will replace the driveshaft free of charge.
Product
HYUNDAI — 2023 HYUNDAI IONIQ 5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V005000·2024-01-01
ABS Remorques semi-trailers recalled for coupling plate deterioration
ABS Remorques is recalling 2014-2023 RC, WC, LRC, and LWC semi-trailers due to coupling plate deterioration that may cause king pin failure and trailer detachment. Detached trailers cannot be controlled and may crash or obstruct traffic.
Product
ABS REMORQUES — 2018 ABS REMORQUES RC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V030000·2024-01-01
2021 Harley-Davidson Motorcycles Instrument Cluster May Fail in Cold Weather
Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.
Product
HARLEY-DAVIDSON — 2021 HARLEY-DAVIDSON RH1250S
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·24071·2023-12-28
High-Powered Magnetic Balls Recalled Due to Ingestion Hazard
A set of 5mm magnetic balls sold online through Walmart.com via Joybuy is being recalled because the magnets are too strong and can cause serious internal injuries or death if swallowed, especially by children.
Product
Relax 5mm Science Kit, Large Hematite Magnets Magnetic Stones Building Blocks
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24069·2023-12-28
BlendJet Recalls 4.8 Million BlendJet 2 Portable Blenders for Fire and Laceration Risk
BlendJet Inc. is recalling approximately 4.8 million BlendJet 2 Portable Blenders because they can overheat, catch fire, or have blades that break off during use, creating fire and laceration hazards.
Product
BlendJet 2 Portable Blenders
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·24070·2023-12-28
Simpson Gas Pressure Washers Recalled for Lithium Battery Burn Hazard
FNA Group is recalling about 2,930 Simpson Gas Pressure Washers with Electric Start because the lithium battery in the electric start system can overheat and pose a burn hazard. Two reports of battery overheating have been received, but no injuries have been reported.
Product
Simpson Gas Pressure Washers with Electric Start
Category
Consumer Product
Distribution
Distributed nationwide

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