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

1101–1125 of 30778

ModerateFDA (Devices)·Z-2037-2026·2026-05-06
Medline medical procedure kits recalled for endotoxin contamination
Medline is recalling medical procedure kits containing Neuro Sponges due to higher-than-expected endotoxin levels. The affected in-market product may be out-of-specification for endotoxin.
Product
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. CATARACT PACK, Medline Kit Number/SKU DYNJ48725A; 2. OCULAR PACK, Medline Kit Number/SKU DYNJ64138B; 3. OCULOPLASTY PACK, Medline Kit Number/SKU DYNJ64572A; 4. OCULOPLASTY PACK, Medli
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1965-2026·2026-05-06
Philips SmartPath to dStream MR Elastography System Reconstruction Error
Philips is recalling certain SmartPath to dStream 1.5T MR Elastography systems due to potential stiffness value errors when specific image reconstruction parameters are used, which may cause incorrect voxel size settings in the default MRE scan protocol.
Product
Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260. 2. Model Number (REF): 782112.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1953-2026·2026-05-06
Philips Achieva 3.0T MR Elastography system stiffness value error recall
Philips is recalling the Achieva 3.0T with MR Elastography system due to potential stiffness value errors in image reconstruction when specific parameters are used, which may cause incorrect voxel size display in the default scan protocol.
Product
Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781278.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1949-2026·2026-05-06
Genius Review Station Display Modified Outside Validated Configuration
Hologic is correcting Genius Review Station displays (model CMP-01669) that were modified by users outside the FDA-cleared configuration. The devices need restoration to validated settings per the manufacturer's Operator's Manual.
Product
Brand Name: Genius" Review Station Product Name: Genius" Review Station Display (Barco Monitor) Model/Catalog Number: CMP-01669 Software Version: N/A - not software version specific Component: Yes, the Genius" Review Station is a component of the Genius" Digital Diagnostics S
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1950-2026·2026-05-06
HiResolution Bionic Ear Battery Pak Fails Safety Door Compliance
Advanced Bionics is recalling HiResolution Bionic Ear System M Zn-Air Battery Paks because the non-tamperproof battery door does not require a tool to open, violating safety standards. The issue affects 45,173 units distributed worldwide.
Product
Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110; CI-5501-120; CI-5501-130; CI-5501-140; CI-5501-150; CI-5501-190; CI-5501-240; CI-5501-250; CI-5501-260; CI-5501-270; CI-5501-280 Software Version: Not Applicable
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1983-2026·2026-05-06
BD GasPak EZ Campy Pouch System Recall for Below-Specification Gas Production
Becton Dickinson & Co. is recalling certain lots of BD GasPak EZ Campy Gas Generating Pouch Systems because gas generating sachets may produce carbon dioxide levels below specification, potentially affecting microbiologic laboratory testing.
Product
BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0500-2026·2026-05-06
iVIZIA Dry Eye Lubricant Drops Recalled for Sterility Assurance
Thea Pharma, Inc. is recalling iVIZIA Dry Eye (Povidone 0.5%) lubricant eye drops nationwide due to the FDA's discovery of manufacturing process deviations that affect the product's sterility assurance.
Product
IVIZIA DRY EYE — IVIZIA DRY EYE (POVIDONE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1998-2026·2026-05-06
Heraeus PALAMIX duo dental mixing system batches worldwide recall
Heraeus Medical is recalling PALAMIX duo dental mixing units (Material Number 66057897) because the mixing rod may come loose from its lock during use in units older than 1.5 years. The shelf life is being reduced from 3 years to 1.5 years.
Product
Heraeus, PALAMIX duo. Material Number: 66057897.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1997-2026·2026-05-06
Heraeus PALAMIX uno Dental Material Mixing Rod Loose Risk Recall
Heraeus Medical is recalling PALAMIX uno dental material because the mixing rod may come loose during mixing in units older than 1.5 years. The shelf life has been reduced from 3 years to 1.5 years.
Product
Heraeus, PALAMIX uno. Material Number: 66057893.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0494-2026·2026-05-06
Levocarnitine Injection USP Missing Label Recall
American Regent, Inc. is recalling Levocarnitine Injection USP (1 g/5 mL) due to missing labeling on certain lots. The affected product was distributed nationwide.
Product
LEVOCARNITINE — LEVOCARNITINE (LEVOCARNITINE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0509-2026·2026-05-06
CVS Lidocaine Wound Gel recalled for failed pH specifications
CVS Lidocaine Wound Gel is being recalled because it failed pH specifications. The affected product is distributed nationwide.
Product
Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·24V378000·2026-05-05
[pending] 2023 GRAND DESIGN SOLITUDE
Pending LLM rewrite. Source: NHTSA 24V378000.
Product
GRAND DESIGN — 2023 GRAND DESIGN SOLITUDE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V283000·2026-05-05
[pending] 2021 TESLA MODEL Y
Pending LLM rewrite. Source: NHTSA 26V283000.
Product
TESLA — 2021 TESLA MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V377000·2026-05-05
[pending] 2025 LION LIONC
Pending LLM rewrite. Source: NHTSA 24V377000.
Product
LION — 2025 LION LIONC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V301000·2026-05-04
[pending] 2022 NEWMAR BAY STAR
Pending LLM rewrite. Source: NHTSA 24V301000.
Product
NEWMAR — 2022 NEWMAR BAY STAR
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-05042026-01·2026-05-04
Giovanni Rana Ravioli Pasta Contains Undeclared Shellfish Allergen
USDA FSIS issued a public health alert for Giovanni Rana ravioli sold at Costco in Maryland and New Jersey. Products labeled as beef and burrata actually contain shrimp in lobster sauce, an undeclared shellfish allergen.
Product
Rana Meal Solutions, LLC — FSIS Issues Public Health Alert for Ravioli Pasta With Beef Sauce Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
2 states
HighNHTSA·25V254000·2026-05-04
[pending] 2025 MERCEDES-BENZ G 580
Pending LLM rewrite. Source: NHTSA 25V254000.
Product
MERCEDES-BENZ — 2025 MERCEDES-BENZ G 580
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V304000·2026-05-04
[pending] 2024 NISSAN SENTRA
Pending LLM rewrite. Source: NHTSA 24V304000.
Product
NISSAN — 2024 NISSAN SENTRA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V302000·2026-05-04
[pending] 2021 MINI COOPER SE
Pending LLM rewrite. Source: NHTSA 24V302000.
Product
MINI — 2021 MINI COOPER SE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V257000·2026-05-04
[pending] 2022 VOLVO VN
Pending LLM rewrite. Source: NHTSA 25V257000.
Product
VOLVO — 2022 VOLVO VN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V128000·2026-05-03
[pending] 2021 TOYOTA HIGHLANDER
Pending LLM rewrite. Source: NHTSA 26V128000.
Product
TOYOTA — 2021 TOYOTA HIGHLANDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V129000·2026-05-03
[pending] 2025 GMC SIERRA 3500
Pending LLM rewrite. Source: NHTSA 26V129000.
Product
GMC — 2025 GMC SIERRA 3500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V160000·2026-05-02
[pending] 2021 JAYCO SWIFT
Pending LLM rewrite. Source: NHTSA 24V160000.
Product
JAYCO — 2021 JAYCO SWIFT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V165000·2026-05-02
[pending] 2024 BMW K 1600 GT
Pending LLM rewrite. Source: NHTSA 24V165000.
Product
BMW — 2024 BMW K 1600 GT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V099000·2026-05-02
[pending] 2022 KIA SOUL
Pending LLM rewrite. Source: NHTSA 25V099000.
Product
KIA — 2022 KIA SOUL
Category
Vehicle
Distribution
Distributed nationwide

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