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

15851–15875 of 27769

HighFDA (Drugs)·D-0064-2024·2023-10-25
Compounded Intranasal Lidocaine-Oxymetazoline Solution Recalled Due to Sterility Assurance
Pine Pharmaceuticals is recalling 860 syringes of intranasal lidocaine-oxymetazoline solution distributed nationwide due to lack of sterility assurance. Lot 67808 expired 10/23/2023.
Product
Lidocaine HCL 2% and Oxymetazoline HCl 0.025% Solution for intranasal administration, 2 mL syringes, Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0048-2024·2023-10-25
Doxil Chemotherapy Drug Recalled for Improper Storage Temperature During Shipment
Baxter Healthcare is recalling 472 vials of Doxil chemotherapy medication due to exposure to temperatures exceeding labeled storage conditions during transportation. Affected vials were distributed nationwide.
Product
DOXIL — DOXIL (DOXORUBICIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0060-2024·2023-10-25
TPC Drops Ophthalmic Solution Recalled for Lack of Sterility Assurance
Pine Pharmaceuticals is recalling TPC Drops ophthalmic solution due to lack of assurance of sterility. The recall affects 1693 droppers distributed nationwide.
Product
TPC Drops (tropicamide 1%- phenylephrine 2.5%- cyclopentolate HCl 1% ophthalmic solution, 5 mL droppers, Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0054-2024·2023-10-25
Calcium Gluconate Inhalation Solution Recalled Due to Sterility Concerns
Pine Pharmaceuticals is recalling Calcium Gluconate 2.5% inhalation solution due to lack of sterility assurance. Patients should stop using affected syringes and contact their healthcare provider.
Product
Calcium Gluconate 2.5% solution for inhalation, 5mL pre-filled syringes, Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0114-2024·2023-10-25
HydroPICC Catheter Kit Recall: Missing Critical Use-Restriction Warnings
Access Vascular is recalling HydroPICC Dual Lumen Catheter kits with incorrect instruction documents that omit critical warnings about adult-only use and vessel sizing. No adverse events have been reported.
Product
HydroPICC 5Fr Dual Lumen, 80cm guidewire - Basic Kit, Product Model Number 80002002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0051-2024·2023-10-25
Vancomycin Intraocular Injection Recalled Due to Sterility Assurance Failure
Pine Pharmaceuticals is recalling 26 vials of Vancomycin 1 MG/0.1 ML intraocular injection (Lot #69985) due to lack of assurance of sterility. The product was distributed nationwide.
Product
Vancomycin 1 MG/0.1 ML Solution for Intraocular Injection, 0.8 ML Single Dose Vial, Rx only, Compounded by: Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0055-2024·2023-10-25
FDA Recalls Compounded Ophthalmic Solution Due to Sterility Concerns
Pine Pharmaceuticals recalls Tropi-Phen ophthalmic solution due to lack of sterility assurance. The 15 mL droppers were distributed nationwide and customers should not use affected lots.
Product
Tropi-Phen (Tropicamide 1% phenylephrine HCl 2.5%) ophthalmic solution, 15 mL multi-use Droppers, Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0059-2024·2023-10-25
Compounded Lidocaine-Phenylephrine Injectable Recalled Due to Sterility Assurance Issues
Pine Pharmaceuticals is recalling 9,673 vials of compounded lidocaine-phenylephrine injectable due to lack of assurance of sterility. Affected lots were distributed nationwide.
Product
Lidocaine-phenylephrine 1%-1.5% 1mL Single Dose Vial, Rx only, Compounded by Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.
Category
Drug
Distribution
Distributed nationwide
CriticalCPSC·24011·2023-10-19
Fortress Safe Biometric Gun Safes: Unauthorized Access and Risk of Death
Xpedition LLC is recalling approximately 61,000 biometric gun safes because the biometric locks can be opened by unauthorized users, posing serious injury and death risks. One death has been reported in a recent lawsuit.
Product
Biometric Gun Safes
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24010·2023-10-19
Thomas & Friends Wooden Railway Troublesome Truck Toys Recalled for Choking and Magnet Ingestion
Fisher-Price is recalling about 21,000 Thomas & Friends Wooden Railway Troublesome Truck train cars because the magnetic connector piece can detach, posing choking and magnet ingestion hazards.
Product
Thomas & Friends Wooden Railway Troublesome Truck & Crates and Thomas & Friends Wooden Railway Troublesome Truck & Paint
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24704·2023-10-19
Polaris RZR Recreational Off-Road Vehicles Recalled for Crash Hazard
Polaris is recalling certain 2023 and 2024 RZR recreational off-road vehicles because an improperly routed brake line can contact the front wheels, causing brake loss and crashes. Consumers should immediately stop using the vehicles and contact a Polaris dealer for a free inspection and repair.
Product
Model Year 2023 RZR PRO XP and PRO XP 4 and Model Year 2024 RZR XP and XP 4 ROVs
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0011-2024·2023-10-18
Ginger Snap Milk Chocolate recalled for undeclared peanut allergen
Dick Taylor Inc is recalling Ginger Snap Milk Chocolate due to undeclared peanut allergen. People with peanut allergies may experience serious allergic reaction if they consume this product.
Product
Ginger Snap Milk Chocolate, 2 oz wrapped
Category
Food
Distribution
0 states
CriticalFDA (Food)·F-0287-2024·2023-10-18
Quaker Pancakes with Whole Grain Oats Recalled for Undeclared Soy Allergen
Comercializadora Pepsico Mexico recalls Quaker Pancakes with Whole Grain Oats due to undeclared soy allergen. The product contains soy not listed on the label, creating a health risk for consumers with soy allergies.
Product
QUAKER PANCAKES WITH WHOLE GRAIN OATS, NET WT 15.97OZ (1LB)
Category
Food
Distribution
0 states
CriticalFDA (Devices)·Z-0028-2024·2023-10-18
FDA Recalls Fresenius 2008T Hemodialysis Systems Due to PCBA Leaching
Fresenius Medical Care is recalling 703 units of the Fresenius 2008T Hemodialysis System nationwide due to potential PCBA (printed circuit board assembly) leaching from machine tubing.
Product
2008T Hemodialysis SYS, with CDX
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0032-2024·2023-10-18
Hemodialysis Machines Recalled Due to Potential PCBA Leaching
Fresenius Medical Care is recalling 733 hemodialysis machines nationwide due to potential printed circuit board material leaking from tubing.
Product
2008T HD SYS. CDX BLUESTAR
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0031-2024·2023-10-18
Medical device manufacturer recalls hemodialysis machines for potential PCBA leaching
Fresenius Medical Care is recalling 733 units of the 2008T GEN 2 Bibag hemodialysis machine due to potential printed circuit board assembly material leaching from tubing. All affected units were distributed domestically.
Product
2008T GEN 2 Bibag without CDX
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0007-2024·2023-10-18
Syringes with Luer Lock Recalled for Blood Backfill and Foreign Material Risk
Fresenius Medical Care is recalling 3ML syringes with Luer Lock due to potential blood backfill leakage and foreign material contamination. The recall affects 124,773 boxes distributed nationwide.
Product
3ML Syringe Luer Lock with needle 20GX1, Part Number 15-03ML-0, 100 per box, 24 boxes per case
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0005-2024·2023-10-18
FDA Recalls Fresenius 10mL Luer Lock Syringes Due to Leakage and Foreign Material
Fresenius Medical Care is recalling 10mL syringes nationwide due to potential blood backfill leakage and foreign material. The recall affects 124,773 boxes of the devices.
Product
10ML SYRINGE LUER LOCK W/OUT NEEDLE, Part Number 15-R010-0, 100 per box, 12 boxes to a case
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0033-2024·2023-10-18
Hemodialysis machines recalled for potential PCBA leaching from tubing
Fresenius Medical Care is recalling 733 units of 2008T HD hemodialysis machines nationwide due to potential PCBA leaching from tubing. The FDA classified this as a Class I recall.
Product
2008T HD SYS. CDX W/BIBAG BLUESTAR
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0042-2024·2023-10-18
FDA recalls BREXAFEMME tablets due to cross-contamination with ezetimibe
The FDA is recalling BREXAFEMME antifungal tablets due to potential cross-contamination with ezetimibe during manufacturing, with two lot numbers distributed nationwide.
Product
BREXAFEMME (Ibrexafungerp) tablets 150 mg, 4 count cartons, Rx Only, Manufactured for and distributed by SCYNEXIS, Inc., Jersey City, NJ 07302 NDC 75788-115-04
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0035-2024·2023-10-18
Hemodialysis Systems Recalled for Potential PCBA Tubing Leaching
Fresenius Medical Care is recalling 733 hemodialysis machines nationwide due to potential leaching of circuit board material from tubing. Affected equipment may contaminate blood or dialysate during treatment.
Product
2008T HD SYS. W/O CDX W/BIBAG BLUESTAR
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0029-2024·2023-10-18
Hemodialysis machines recalled for potential printed circuit board contamination
Fresenius Medical Care is recalling 733 2008T Hemodialysis Systems without CDX due to potential PCBA leaching from tubing. This FDA Class I recall affects units distributed nationwide.
Product
2008T Hemodialysis System without CDX
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0034-2024·2023-10-18
Hemodialysis machines recalled due to potential circuit board material leaching
Fresenius Medical Care is recalling 733 units of 2008T hemodialysis systems nationwide due to potential leaching of printed circuit board assembly material from tubing. No illnesses or injuries have been reported.
Product
2008T HD SYS. W/O CDX BLUESTAR
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0006-2024·2023-10-18
10ML Syringe Luer Lock Recalled for Potential Blood Backfill Leakage
Fresenius Medical Care is recalling 124,773 boxes of 10ML Syringe Luer Lock syringes due to potential blood backfill leakage and foreign material contamination.
Product
10ML SYRINGE LUER LOCK W/NEEDLE, Part Number 15-10ML-0, 100 per box, 12 boxes per case
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0007-2024·2023-10-18
LuLu Chinese Express Korean Noodles Recalled for Undeclared Egg Allergen
LuLu Chinese Express Korean Noodles (Japchae) with Vegetables are being recalled due to undeclared egg allergen. The 54 containers distributed in Missouri may pose a health risk to consumers with egg allergies.
Product
LuLu Chinese Express Korean Noodles (Japchae) w/ Vegetables. Net Wt 16oz.
Category
Food
Distribution
1 state

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