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

1076–1100 of 90235

SevereFDA (Devices)·Z-2889-2026·2026-08-12
Beckman Coulter MicroScan Panel Update DVD Kits Recalled
Beckman Coulter is recalling MicroScan LabPro V5.03 Panel Update 11 DVD Kits due to incorrect algorithms that may affect antimicrobial susceptibility test results, potentially leading to false susceptibility classifications.
Product
REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the following instruments: - B1018-280 MicroScan autoSCAN-4 Instrument - B1018-283 MicroScan WalkAway-40 plus Instrument - B1018-284 MicroScan WalkAway-96 plus Instrument - B1018-440 DxM-1040 MicroScan…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1216-2026·2026-08-12
Smoked Cheddar Cheese Varieties Recalled Due to Listeria Contamination
Clover Hill Dairy is recalling its smoked cheddar cheese varieties because they may be contaminated with Listeria monocytogenes. The products were sold in Maryland, Virginia, and New York.
Product
Clover Hill Dairy LLP, Smoked Cheddar Cheese Varieties (Cheddar, White Cheddar). Sold in 1/2-lb and 1-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Food)·H-1214-2026·2026-08-12
Clover Hill Dairy Pepper Jack Cheese Varieties Recalled Due to Listeria Contamination
Clover Hill Dairy, LLC is recalling certain Pepper Jack Cheese Varieties because they may be contaminated with Listeria monocytogenes.
Product
Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (Snack Pack Assorted Pepperjack Stix (Jalapeno Cheddar, Pepper Jack)). Sold in approximate 0.40-lb (6.4oz) units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2900-2026·2026-08-12
GEM Premier 5000 PAK Lysing Solution Concentration Recall
Specific lots of the GEM Premier 5000 PAK lysing bag solution have an active ingredient concentration that does not meet manufacturing specifications, which could delay recognition and management of Co-Oximetry and total bilirubin abnormalities.
Product
GEM Premier 5000 PAK Part Numbers: 00055360010 00055360011 00055407504 00055415010 00055430010 00055430011 00055445010 00055445011 00055360010.A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2897-2026·2026-08-12
United Orthopedic U2 Knee Implant Bushings Recalled Over Engraving Design Issue
United Orthopedic Corp. is recalling three Femoral offset bushing components of the U2 Total Knee System due to a design issue causing incorrect engraved numbering that could lead to incorrect implant orientation during surgery.
Product
Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 0mm and 4mm Model/Catalog Number: 9323-5310 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No, N/A
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V524000·2026-08-12
BMW X3 Vehicles Recalled Due to Potential Loss of Steering Control
BMW is recalling certain 2024-2026 X3 models because the steering spindle may be incorrectly attached to the steering column, increasing crash risks.
Product
BMW — BMW X3
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-1205-2026·2026-08-12
Clover Hill Dairy Mild Cheese Varieties Recalled Due to Listeria Contamination
Clover Hill Dairy, LLC is recalling various mild cheese varieties because they may be contaminated with Listeria monocytogenes.
Product
Clover Hill Dairy LLP, Mild Cheese Variety (Yummy Cheddar, White Cheddar, White Colby, Monterey Jack, Marble Jack). Sold in 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2909-2026·2026-08-12
Blom-Singer Voice Prosthesis Boxes Mislabeled with Wrong Flange Type
Freudenberg Medical is recalling 12 Blom-Singer Classic Indwelling Voice Prosthesis devices because the boxes are mislabeled, swapping Large Esophageal Flange and Large Esophageal and Tracheal Flange contents.
Product
Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm REF: 1610-LEF
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2854-2026·2026-08-12
Copan WASPLab Software Recall Over Results Overwrite Issue
Copan WASP is recalling WASPLab devices due to a software issue in the WebApp that may prevent users from overwriting results. The recall affects WebApp versions 2.33.1, 2.33.3, and 2.34.2.
Product
Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1, 2.33.3 and 2.34.2 Product Description: WASPLab is an automated device intended to be used for the incubation and the digital imaging of agar culture plates streaked…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1212-2026·2026-08-12
Clover Hill Dairy Flavored Cheese Recalled Due to Listeria Contamination
Clover Hill Dairy, LLC is recalling Old Bay Cheddar flavored cheese because it may be contaminated with Listeria monocytogenes.
Product
Clover Hill Dairy LLP, Flavored Cheese (Old Bay Cheddar). Sold in approximate 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Drugs)·D-0744-2026·2026-08-12
Cyclophosphamide Injection Recall: Stainless Steel Particulate Matter Found
Cyclophosphamide for Injection, USP, 2 gram/vial, is being recalled due to the presence of particulate matter identified as stainless steel. The recall affects 1,464 vials distributed nationwide.
Product
Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8114-1
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1218-2026·2026-08-12
Salvadorean Cheese Recalled for Possible Listeria Contamination
La Colonia Foods LLC is recalling Selectos Latinos Requeson Salvadoreno Ricotta Style Salvadorean Cheese (14 oz) due to possible contamination with Listeria monocytogenes.
Product
Selectos Latinos Requeson Salvadoreno Ricotta Style Salvadorean Cheese, Net Weight 14 oz, packed into retail-sized clear plastic containers. Keep refrigerated.
Category
Food
Distribution
2 states
SevereFDA (Food)·H-1203-2026·2026-08-12
Clover Hill Dairy Cuajada Recalled Due to Listeria Contamination
Clover Hill Dairy, LLC is recalling vacuum-sealed cuajada due to Listeria monocytogenes contamination. The product was distributed in MD, VA, and NY.
Product
Clover Hill Dairy LLP, Cuajada (vacuum sealed), sold in 30-lb boxes. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Food)·H-1211-2026·2026-08-12
Clover Hill Dairy LLP Flavored Horseradish Cheese Recalled Due to Listeria Contamination
Clover Hill Dairy, LLC is recalling flavored horseradish cheese because it may be contaminated with Listeria monocytogenes.
Product
Clover Hill Dairy LLP, Flavored Cheese (horseradish). Sold in approximate 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
Category
Food
Distribution
3 states
SevereFDA (Drugs)·D-0745-2026·2026-08-12
FDA Recalls Mirabegron Tablets Over Nitrosamine Impurity
Zydus Pharmaceuticals is recalling Mirabegron extended-release tablets, 25 mg, due to an out-of-specification result for the N-Nitroso Mirabegron impurity. The recall affects nationwide distribution in the USA.
Product
MIRABEGRON — MIRABEGRON (MIRABEGRON)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1219-2026·2026-08-12
Selectos Latinos Requeson Mexicano Cheese Recalled for Listeria Risk
La Colonia Foods LLC is recalling 169 units of Selectos Latinos Requeson Mexicano Mexican Cottage Cheese (16 oz) due to potential contamination with Listeria monocytogenes. The product was distributed in MD and VA.
Product
Selectos Latinos Requeson Mexicano Mexican Cottage Cheese, Net Weight 16 oz, packed into retail-sized clear plastic containers. Keep refrigerated.
Category
Food
Distribution
2 states
HighFDA (Food)·H-1198-2026·2026-08-12
Frozen Flounder Sashimi with Sauce Recalled Due to Undeclared Allergens
Eunha Fisheries Co., LTD is recalling Frozen Flounder Sashimi with Sauce because it contains undeclared wheat, soy, sesame, Yellow #5, and Blue #1.
Product
FLOUNDER SASHIMI WITH SAUCE; Keep Frozen; Net WT: 300g; UPC: 8 809342 366186
Category
Food
Distribution
2 states
HighFDA (Food)·H-1197-2026·2026-08-12
Frozen Halibut Slices Recalled Due to Undeclared Wheat, Soy, and Sesame
Eunha Fisheries Co., LTD is recalling Sliced Korean Halibut due to undeclared allergens including wheat, soy, and sesame.
Product
Sliced Korean Halibut with Soy sauce, Wasabi, Vinegar Chili Paste; Keep Frozen; Net WT: 12.2OZ (374g); UPC: 6 78108 16991 4
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-2870-2026·2026-08-12
Intramedullary Bone Saw Blade Assembly Recall for Packaging Damage
Zimmer Biomet recalls Intramedullary Bone Saw Blade Assemblies due to potential sterile barrier packaging damage from exposed saw blades. FDA Class II medical device recall.
Product
Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description: Intramedullary Bone Saw Blade Assembly 15mm
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2834-2026·2026-08-12
REMISOL Advance Software Version 2.5 Recalled for Incorrect Test Result Reporting
Beckman Coulter Biomedical GmbH is recalling REMISOL Advance Software Version 2.5 because it may incorrectly report combo assay test outcomes.
Product
REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info REMISOL Advance Data Manager collects and manages data and workflow for 128 connections
Category
Medical Device
Distribution
5 states
HighFDA (Devices)·Z-2842-2026·2026-08-12
Quantum Outback Powered Wheelchair Controller Recalled Due to Unexpected Braking Risk
Pride Mobility Products Corp. is recalling Quantum Outback powered wheelchairs due to a software issue that may cause unexpected braking and potential injury.
Product
Brand Name: Quantum Rehab Product Name: Quantum Outback Model/Catalog Number: Quantum Outback Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1221-2026·2026-08-12
Korean Soybean Paste Recalled for Undeclared Fish Allergen
JINA F&C is recalling 4,153 units of Wangshin Doenjang soybean paste because the label does not list anchovy (fish) as an ingredient, posing an allergen risk to consumers with fish allergies.
Product
Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Premium Soybean Paste UPC: 8 809897 940169
Category
Food
Distribution
0 states
HighNHTSA·26E056000·2026-08-12
Odyne Recalls Hybrid Systems Due to Traction Battery Fire Risk
Odyne Systems is recalling certain hybrid systems with specific part numbers because the high-voltage batteries may fail, increasing the risk of a fire.
Product
ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2845-2026·2026-08-12
Powered Wheelchair Controller Software May Cause Unexpected Brake Stop
Pride Mobility is recalling 1,102 Q6 Edge HD powered wheelchairs due to a software issue in the controller that may cause unexpected park brake stops or system crashes when reminder pop-ups appear during use.
Product
Brand Name: Quantum Rehab Product Name: Q6 Edge HD Model/Catalog Number: Q6 Edge HD Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2888-2026·2026-08-12
MicroScan LabPro V5.03 Panel Update 11 analyzers recalled for incorrect algorithms affecting test results
The FDA is recalling MicroScan LabPro V5.03 Panel Update 11 electronic analyzers because their algorithms may produce inaccurate antimicrobial susceptibility test results.
Product
REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US), Electronic installed on the following instruments: - B1018-280 MicroScan autoSCAN-4 Instrument - B1018-283 MicroScan WalkAway-40 plus Instrument - B1018-284 MicroScan WalkAway-96 plus Instrument - B1018-440…
Category
Medical Device
Distribution
Distributed nationwide

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1076–1100 of 90235