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

3976–4000 of 39749

SevereFDA (Devices)·Z-2588-2024·2024-09-04
Smiths Medical Bivona Tracheostomy Tubes Recalled for Flange Tear Risk
Smiths Medical is recalling PORTEX Bivona Tracheostomy Tubes due to a manufacturing defect that may cause the securement flange to tear. Affected lots include neonatal, pediatric, and adult sizes distributed worldwide with 177,340 units impacted.
Product
PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS TRACHEOSTOMY TUBE 7.0MM TIGHT TO SHAFT CUFF, Product Code/List Number/Item Code 670170; b) TTS TRACHEOSTOMY TUBE 8.0MM TIGHT TO SHAFT CUFF 1/EA, Product Code/List Number/Item Code 670180
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2603-2024·2024-09-04
Tracheostomy Tubes Recalled for Manufacturing Defect Affecting Securement Flange
Smiths Medical recalled specific lots of PORTEX Bivona Tracheostomy Tubes due to a manufacturing defect that may cause the securement flange to tear. Affected products were distributed worldwide.
Product
PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) NEONATAL TRACHEOSTOMY TUBE , Product Code/List Number/Item Code 65N025; b) NEONATAL TRACHEOSTOMY TUBE , Product Code/List Number/Item Code 65N030; c) NEONATAL TRACHEOSTOMY TUBE , Product Code/List Number/Item Code…
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2604-2024·2024-09-04
Bivona Tracheostomy Tubes Recalled for Manufacturing Defect in Securement Flange
Smiths Medical recalls specific lots of Bivona Neonatal/Pediatric and Adult Tracheostomy Tubes worldwide due to a manufacturing defect that may cause the securement flange to tear.
Product
PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) PAED. TRACHEOSTOMY TUBE 2.5MM AIRE-CUF , Product Code/List Number/Item Code 65P025; b) PAED. TRACHEOSTOMY TUBE 3.0MM AIRE-CUF , Product Code/List Number/Item Code 65P030; c) PAED, TRACHEOSTOMY TUBE 3.5mm AIRE-CUF…
Category
Medical Device
Distribution
0 states
SevereUSDA FSIS·025-2024·2024-08-30
Hickory Hollow Jerky Recalls Beef and Bacon Jerky Produced Without Inspection
Hickory Hollow Jerky is recalling approximately 6,229 pounds of beef and bacon jerky produced without federal inspection. The products were distributed in five states and online.
Product
Hickory Hollow Jerky — Hickory Hollow Jerky Recalls Ready-To-Eat Jerky Products Produced Without Benefit of Inspection
Category
Food
Distribution
5 states
SevereNHTSA·24V646000·2024-08-30
E-One Recalls Cyclone and Typhoon Vehicles Due to Crossmember Defect
E-One is recalling 2022-2024 Cyclone and Typhoon vehicles because a broken engine crossmember can damage the cooling fan, potentially causing an engine stall and increasing crash risk.
Product
E-ONE — E-ONE CYCLONE II, CYCLONE N, TYPHOON N
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·24350·2024-08-29
HALO 1000 Portable Power Stations Recalled for Fire and Burn Hazards
About 5,740 HALO 1000 Portable Power Stations are recalled because their lithium-ion batteries can overheat and catch fire. One death from smoke inhalation and four fire incidents have been reported.
Product
HALO 1000 Portable Power Stations
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24352·2024-08-29
Glow in Dark Party Supplies Toy Sets Recalled for Battery Ingestion Hazard
Glow in Dark Party Supplies Toy Sets sold on Amazon contain button cell batteries in Bunny Ears Headbands that can be easily accessed by children, posing a serious ingestion hazard. The sets violate federal battery-operated toy regulations.
Product
Glow in Dark Party Supplies Toy Sets
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2636-2024·2024-08-28
McGrath Mac Video Laryngoscope battery depletion may cause thermal event and explosion
McGrath Mac Video Laryngoscope devices may experience battery management system failures causing batteries to deplete below design thresholds, potentially resulting in thermal events and explosions.
Product
McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0641-2024·2024-08-28
Acetaminophen Aspirin Caffeine Tablets Recalled for Missing Drug Facts Labels
Aurohealth LLC is recalling Acetaminophen, Aspirin and Caffeine tablets because some bottles are missing the manufacturer's label containing drug facts information. Affected product was distributed in NJ, NY, and PA.
Product
ACETAMINOPHEN ASPIRIN AND CAFFEINE — ACETAMINOPHEN ASPIRIN AND CAFFEINE (ACETAMINOPHEN, ASPIRIN AND CAFFEINE)
Category
Drug
Distribution
3 states
SevereFDA (Devices)·Z-2587-2024·2024-08-28
ClotTriever XL Catheter instructions updated to prevent device entrapment and embolism
Inari Medical has updated instructions for the ClotTriever XL Catheter (30 mm) to prevent device entrapment and pulmonary embolism. Approximately 2,488 units distributed worldwide are affected.
Product
ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Reference: IU-01011
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1788-2024·2024-08-28
Meijer Dunking Cookies Recalled for Undeclared Milk Allergen
Meijer Inc is recalling Meijer Dunking Cookies Chocolate Chip (10 oz) due to undeclared milk. The product poses a risk to consumers with milk allergies.
Product
MEIJER DUNKING COOKIES CHOCOLATE CHIP, 10oz in clear plastic container. UPC 7-13733-71297-2
Category
Food
Distribution
6 states
SevereNHTSA·24V643000·2024-08-28
Volkswagen ID.4 passenger airbag inflator fasteners may be loose
Volkswagen is recalling certain 2023-2024 ID.4 vehicles because the fasteners securing the passenger frontal airbag inflator may be loose, so the airbag may not deploy as intended.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0635-2024·2024-08-28
FDA Recalls Acetaminophen Injection Due to Labeling Mix-up
Hikma Pharmaceuticals is recalling Acetaminophen Injection because bags of Dexmedetomidine HCl were found packaged inside Acetaminophen-labeled overWraps. The error could result in patients receiving the wrong intravenous medication.
Product
ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
Category
Drug
Distribution
2 states
SevereFDA (Devices)·Z-2637-2024·2024-08-28
McGRATH MAC EMS Video Laryngoscope Battery Management System Recall
Covidien is recalling McGRATH MAC EMS Video Laryngoscopes due to a battery management system defect that may deplete below design specifications, creating risk of thermal events and explosion. About 10,449 units were distributed worldwide.
Product
McGRATH" MAC EMS Video Laryngoscope, REF: 300-200-000 , Non-Sterile, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0638-2024·2024-08-28
FDA Class I Recall: B. Braun Sodium Chloride Injection for Particulate Matter
B. Braun Medical Inc. is recalling 63,444 containers of 0.9% Sodium Chloride Injection USP nationwide due to the presence of particulate matter. This intravenous medication may pose a serious health risk if administered to patients.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·24E072000·2024-08-26
USK Internacional Recalls Tie Rod and Drag Link Assemblies
USK Internacional is recalling certain tie rod and drag link assemblies due to improperly heat-treated ball studs that may break, potentially causing a loss of steering control.
Product
STEERING:LINKAGES:TIE ROD ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V633000·2024-08-23
Jaguar Recalls 2019 I-PACE Vehicles Due to High-Voltage Battery Overheating Risk
Jaguar is recalling 2,760 2019 I-PACE vehicles because the high-voltage battery may overheat, increasing the risk of a fire. Owners should park outside and limit charging to 80% until repairs are complete.
Product
JAGUAR — JAGUAR I-PACE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V637000·2024-08-23
Great Dane Recalls 2025 Everest SS Trailers Due to Welding Defect
Great Dane is recalling 2025 Everest SS refrigerated trailers because improperly welded support gear bracing mounts may cause the trailer to collapse.
Product
GREAT DANE — GREAT DANE EVEREST SS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V629000·2024-08-22
Salem and Wildwood trailer tires may contact chassis components and fail
Forest River is recalling certain 2024-2025 Salem SBF325RL and Wildwood WBF325RL travel trailers because the tires may contact chassis components, causing tire failure.
Product
FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V632000·2024-08-22
McNeilus Recalls 2015-2024 Zero Radius Trucks Due to Side Loader Arm Defect
McNeilus is recalling 2015-2024 Zero Radius refuse trucks because the side loader arm may not be properly secured, increasing crash risk.
Product
MCNEILUS — MCNEILUS ZERO RADIUS
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·24347·2024-08-22
Head Rush Technologies TRUBLUE Speed Auto Belay Devices Fall Hazard
Head Rush Technologies is recalling about 220 TRUBLUE Speed Auto Belay Devices because the backup brake can fail to activate, posing a fall hazard and risk of serious injury or death. Consumers should immediately stop using the devices and contact the manufacturer for a free inspection and repair.
Product
TRUBLUE Speed Auto Belay Devices
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·24V628000·2024-08-22
Forest River trailer tires may contact the outrigger and fail
Forest River is recalling certain 2024 Salem and Wildwood travel trailers because the tire may contact the outrigger, causing the tire to fail. 34 units are affected.
Product
FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1709-2024·2024-08-21
Green peppers recalled due to potential Listeria contamination
RS Hanline and Company Inc is recalling Freshire Farms green peppers due to potential Listeria monocytogenes contamination. The recall affects 850 cases distributed across nine states.
Product
Freshire Farms - Green Peppers packaged in plastic bags containing 3 peppers, 16 bags per case
Category
Food
Distribution
9 states
CriticalFDA (Food)·F-1707-2024·2024-08-21
Freshire Farms jalapenos recalled for potential Listeria monocytogenes contamination
Freshire Farms jalapenos packaged in 8-ounce bags are being recalled due to potential contamination with Listeria monocytogenes. The recall affects 2,298 cases distributed across nine states.
Product
Freshire Farms - Jalapenos packaged in plastic bags at 8oz, 18 bags per case
Category
Food
Distribution
9 states
SevereFDA (Food)·F-1732-2024·2024-08-21
Lunds & Byerlys Fresh Guacamole Dip Recalled for Listeria Contamination
Metro Produce Distributors is recalling Lunds & Byerlys Fresh Guacamole Dip due to potential Listeria monocytogenes contamination. The affected product has a Use By date of 02-AUG-24 and was distributed in Minnesota.
Product
Lunds & Byerlys Fresh Guacamole Dip, Net Wt 14 oz (396g). UPC 0 72431-66072 6. Keep Refrigerated.
Category
Food
Distribution
1 state

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