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

13676–13700 of 31490

HighFDA (Drugs)·D-0489-2024·2024-05-15
TraMADol HCl 50 mg Tablets Recalled for Foreign Baclofen Tablets
RemedyRepack Inc. is recalling TraMADol HCl 50 mg tablets nationwide after a pharmacist discovered a baclofen tablet in a tramadol bottle. Taking the wrong medication poses serious health risks.
Product
TraMADol HCl 50 mg Tablet, Packaged as (a) 30-count blister pack, NDC 70518-3824-00; (b) 90-count blister pack, NDC 70518-3824-02; (a) 180-count blister pack, NDC 70518-3824-03; RX ONLY, MFG: Advagen Pharma Limited, Plainsboro. NJ 08536, Repackaged by: RemedyRepack Inc., Indiana,
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1765-2024·2024-05-15
Vascular Access Catheter Recall Due to Metal Shaving Risk
Angiodynamics is recalling 65 DURAFLOW 2 vascular access devices distributed in Virginia due to potential loose metal shavings that could enter the bloodstream and require surgical removal.
Product
DURAFLOW 2, 28CM STRAIGHT VASC-PAK PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012195
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1763-2024·2024-05-15
Duraflow 2 vascular catheter kit recalled for loose metal shavings
Angiodynamics Inc. is recalling DURAFLOW 2 vascular catheter kits used for hemodialysis and apheresis access due to potential metal shavings that may detach and travel through the vascular system, potentially requiring surgical removal.
Product
DURAFLOW 2, 55CM STRAIGHT BASIC KIT PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012115
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1783-2024·2024-05-15
GE Healthcare Allia IGS Fluoroscopic Systems Recall: Missing Adhesive
GE Healthcare recalls Allia IGS and related interventional fluoroscopic x-ray systems due to potentially missing adhesive on bolts. The defect could allow the detector/elevator or x-ray tube in the gantry assembly to fall.
Product
GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1220-2024·2024-05-15
Martinelli's Gold Medal Apple Juice Recalled for Elevated Inorganic Arsenic
S Martinelli & Company is recalling Martinelli's Gold Medal Apple Juice (1 Liter) due to elevated levels of inorganic arsenic. The affected product has Best By dates of March 9, 2026 or March 10, 2026.
Product
Martinelli's Gold Medal Apple Juice From U.S. Grown Fresh Apples 1 Liter (33.8 fl oz.) No Additives of Any Kind UPC 0 00 41244 00102 6
Category
Food
Distribution
35 states
HighFDA (Devices)·Z-1781-2024·2024-05-15
GE Allia IGS Fluoroscopic X-Ray Systems Adhesive Bolt Defect
GE Healthcare recalled certain Allia IGS and related fluoroscopic x-ray systems due to potential incomplete adhesive on bolts in the gantry assembly, risking detector or tube failure.
Product
GE Healthcare Allia IGS 7 OR, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1771-2024·2024-05-15
DURAMAX vascular catheter recalled for possible metal shaving hazard
The DURAMAX STACKED TIP vascular catheter may contain loosely affixed metal shavings that could embolize and require surgical removal. Lot 5807208 affected, 15 units.
Product
DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK, 1-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028191
Category
Medical Device
Distribution
1 state
HighFDA (Drugs)·D-0484-2024·2024-05-15
Prescription Duloxetine 60 mg capsules recalled for N-nitroso impurity
Breckenridge Pharmaceutical is recalling Duloxetine 60 mg capsules due to elevated levels of N-nitroso-duloxetine, a manufacturing impurity above FDA limits. No illnesses have been reported.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1777-2024·2024-05-15
GE Healthcare X-Ray Systems Recalled for Loose Bolts on Gantry Assembly
GE Healthcare is recalling x-ray imaging systems because adhesive on critical bolts may not have been applied, potentially causing the detector or x-ray tube to fall. The recall affects 21 units worldwide.
Product
GE Healthcare Innova IGS 5, computed tomography x-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1764-2024·2024-05-15
DURAFLOW 2 Vascular Access Device Recalled for Loose Metal Shavings
Angiodynamics is recalling DURAFLOW 2 vascular access devices due to loose metal shavings that may travel through blood vessels, potentially requiring surgical removal.
Product
DURAFLOW 2, 24CM STRAIGHT VASC-PAK PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012185
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1770-2024·2024-05-15
Vascular access device recalled for potential metal shavings embolism risk
Angiodynamics recalls DURAMAX STACKED TIP vascular access devices that may contain loosely affixed metal shavings. Metal shavings could embolize and potentially require surgical removal.
Product
DURAMAX STACKED TIP 32CM STR. BASIC KIT, 5-UP PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103028055
Category
Medical Device
Distribution
1 state
HighFDA (Food)·F-1229-2024·2024-05-15
Belgian Yummies Ice Cream Gelato Recalled for Undeclared Yellow #5 Allergen
Belgian Yummies Homemade Ice Cream Birthday Cake Gelato is being recalled because it contains undeclared Yellow #5, an allergen not listed on the label. The recall affects products distributed in Florida.
Product
Belgian Yummies Homemade Ice Cream Birthday Cake Gelato. Packaged in 5 Liter gray carapina liner.
Category
Food
Distribution
0 states
HighFDA (Food)·F-1218-2024·2024-05-15
Sacramento Cookie Factory Recalls Wine Wafers for Undeclared Milk Allergen
Sacramento Cookie Factory is recalling California Wine Wafer - Mocha Chocolate products because they contain undeclared milk, a common allergen. The recall affects retail packages distributed across multiple U.S. states.
Product
California Wine Wafer - Mocha Chocolate and Original Wine Wafer - Mocha Chocolate [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]
Category
Food
Distribution
14 states
HighFDA (Food)·F-1225-2024·2024-05-15
DB Yummers Barbecue Sauce Recalled Due to Improper Thermal Processing
DB Yummers Sweet & Smokey Barbecue Sauce is recalled for lacking FDA-approved heat treatment. Bottles with best-by dates 05/18/25, 05/26/25, or 08/30/25 distributed in Kentucky and Ohio should not be consumed.
Product
DB Yummers Sweet & Smokey Barbeque Sauce packaged in 19.5 glass bottles, 12 bottles per case, UPC 74872001101.
Category
Food
Distribution
0 states
HighFDA (Drugs)·D-0483-2024·2024-05-15
Duloxetine delayed-release capsules recalled for manufacturing impurity exceeding limits
Breckenridge Pharmaceutical recalls Duloxetine 20 mg capsules nationwide after detecting N-nitroso-duloxetine impurity above FDA-recommended limits in approximately 7,188 units from lot 220456, expiring February 2025.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1215-2024·2024-05-15
Java Wafer Cookies Recalled for Undeclared Milk Allergen
Sacramento Cookie Factory is recalling Java Wafer - Mocha Hazelnut cookies because they contain undeclared milk, a common allergen that poses a health risk to people with milk allergies.
Product
Java Wafer - Mocha Hazelnut [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]
Category
Food
Distribution
14 states
HighFDA (Drugs)·D-0482-2024·2024-05-15
Duloxetine prescription capsules recalled for N-nitroso impurity exceeding FDA limits
Breckenridge Pharmaceutical recalls Duloxetine 30mg delayed-release capsules nationwide due to N-nitroso-duloxetine impurity exceeding FDA-recommended interim limits. The impurity was identified as a CGMP manufacturing deviation.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1216-2024·2024-05-15
Tea Wafers with Vanilla Almond Recalled for Undeclared Milk
Sacramento Cookie Factory recalled Tea Wafers with Vanilla Almond flavor due to undeclared milk allergen. The product was distributed to multiple states and may pose a risk to consumers with milk allergies.
Product
Tea Wafer - Vanilla Almond [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]
Category
Food
Distribution
14 states
HighFDA (Devices)·Z-1780-2024·2024-05-15
GE Healthcare Allia IGS 7 X-ray Systems Adhesive Bolt Failure Recall
GE Healthcare is recalling Allia IGS 7 interventional x-ray systems due to potential adhesive failure on bolts securing the detector and x-ray tube, which could fall during use.
Product
GE Healthcare Allia IGS 7, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1782-2024·2024-05-15
GE Healthcare X-ray Systems: Potential Adhesive Failure Poses Fall Hazard
GE Healthcare is recalling certain Allia and Discovery IGS x-ray systems due to potential adhesive failure that could cause the detector, elevator, or x-ray tube to fall. No injuries reported.
Product
GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1223-2024·2024-05-15
Goya Red Kidney Beans Recalled for Swollen and Leaking Cans
Tradewind Foods de Puerto Rico Inc. is recalling Goya Red Kidney Beans due to swollen and leaking cans discovered during an FDA inspection. The affected product was distributed in Puerto Rico and St. Croix.
Product
Goya Red Kidney Beans, Net Wt.15.5oz.(439g), metal (tin) cans, 24 cans/15.5 oz. per case
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-1762-2024·2024-05-15
Hemodialysis Vascular Access Kit Recalled for Loose Metal Shavings
Angiodynamics DURAFLOW 2 hemodialysis kits may contain loosely affixed metal shavings that could enter the bloodstream. Metal fragments may require surgical removal if they embolize.
Product
DURAFLOW 2, 32CM STRAIGHT BASIC KIT PG-Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012035
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1759-2024·2024-05-15
Randox Clinical Chemistry Calibration Serum Recalled for Measurement Bias
Randox Laboratories has recalled Clinical Chemistry Calibration Serum (Cal2351/Cal10388) due to negative bias in inorganic phosphate measurements on RX Series instruments. The issue could affect the accuracy of clinical chemistry test results.
Product
Clinical Chemistry Calibration Serum (Catalog number Cal2351) that is 20x5ml lyophilized human based serum covering 38 commonly used clinical chemistry tests.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1758-2024·2024-05-15
Spinal Fusion Device Recall: Setscrew Insertion and Tightening Issues
SPINEART's PERLA TL 25D spinal fusion screws are being recalled due to difficulties with setscrew insertion inside the screw head. The setscrew may not be properly tightened or may be positioned incorrectly, potentially affecting spinal stability.
Product
PERLA TL 25D SCREW REF: TLF-DS 45 25-S TLF-DS 45 30-S TLF-DS 45 35-S TLF-DS 45 40-S TLF-DS 45 45-S TLF-DS 55 30-S TLF-DS 55 35-S TLF-DS 55 40-S TLF-DS 55 45-S TLF-DS 65 35-S TLF-DS 65 40-S TLF-DS 65 45-S TLF-DS 65 50-S The PERLA¿ TL system is intended to provide
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1778-2024·2024-05-15
GE Innova IGS Fluoroscopic X-Ray Systems Adhesive Defect Recall
GE Healthcare is recalling certain Innova IGS x-ray systems due to potential adhesive defects on component bolts. Missing adhesive could cause the detector or x-ray tube to fall during use.
Product
GE Healthcare Innova IGS 6, Interventional fluoroscopic x-ray systems
Category
Medical Device
Distribution
Distributed nationwide

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13676–13700 of 31490