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

2676–2700 of 6105

SevereFDA (Devices)·Z-2431-2023·2023-09-06
Cardiosave Hybrid Intra-Aortic Balloon Pump charging issue recall
The Cardiosave Hybrid Intra-Aortic Balloon Pump console fails to charge if not fully inserted into the hospital cart. Users unaware of this requirement may attempt to use a non-charged device during critical cardiac care.
Product
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-08
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1476-2023·2023-09-06
Stonewall Kitchen Peanut Butter Maltballs Recalled for Undeclared Allergens
Stonewall Kitchen brand Peanut Butter Maltballs (6oz) may contain undeclared peanut, soy, and wheat. Consumers with allergies to these ingredients should not consume this product.
Product
Stonewall Kitchen brand Peanut Butter Maltballs packaged in 6oz clear plastic packaging
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-2432-2023·2023-09-06
Cardiosave Rescue Intra-Aortic Balloon Pumps Fail to Charge When Improperly Inserted
Datascope Corp. is recalling 9,175 units of Cardiosave Rescue IABP devices because batteries will not charge if the console is not fully inserted into the hospital cart. Users were often unaware of this insertion requirement.
Product
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1150-2023·2023-09-06
Vegetal Vigra Capsules Recalled for Containing Unapproved Sildenafil
The FDA is recalling Vegetal Vigra 200mg capsules nationwide because they contain sildenafil, an active ingredient in FDA-approved medications. The product was marketed without FDA approval.
Product
Vegetal Vigra, 200mg capsules, 8-count bottle, Manufacturer: Hand-shaking (Int'l) Corp. USA ADD: Hand-shaking Mansion, the 5th Ave., Stanford, USA. UPC 8 931028 556885
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2438-2023·2023-09-06
Cardiosave Rescue Intra-Aortic Balloon Pumps Recalled Due to Autofill Failure
Datascope Corp. is recalling 9,175 Cardiosave Rescue Intra-Aortic Balloon Pumps due to autofill failures that can cause the pump to stop.
Product
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2467-2023·2023-09-06
EVIS EXERA III Duodenovideoscope Recalled Due to Patient Infection Reports
Olympus Corporation recalls 6,426 units of the EVIS EXERA III Duodenovideoscope (Model TJF-Q190V) due to recent reports of patient infections. The device was distributed nationwide in the United States.
Product
EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2435-2023·2023-09-06
Intra-Aortic Balloon Pumps recalled for unexpected gas loss and gain alarms
Datascope's Cardiosave Hybrid Intra-Aortic Balloon Pumps may trigger unexpected alarms indicating gas loss or gain due to undocumented causes including patient movement and blood in the circuit. The FDA Class I recall affects 9,175 units.
Product
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-08
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2437-2023·2023-09-06
Cardiosave Hybrid Intra-Aortic Balloon Pumps recalled for autofill failure
Datascope Corp. is recalling Cardiosave Hybrid intra-aortic balloon pumps due to autofill failure causing pump stops. The FDA Class I recall affects approximately 9,175 units distributed nationwide.
Product
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-08
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2434-2023·2023-09-06
Cardiosave Rescue IABP Pumps Recalled for System Overheating and Pump Failure
Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to system overheating alarms that can cause loss of pumping function and device shutdown.
Product
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85, 0998-UC-0800-75, 0998-UC-0800-83, 0998-UC-0800-85,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2433-2023·2023-09-06
Cardiosave Hybrid IABP devices recalled for temperature and pumping function failures
Datascope is recalling Cardiosave Hybrid intra-aortic balloon pumps due to reported temperature alarms that can cause loss of pumping function or unexpected standby mode. Users have reported these system failures in critical cardiac support devices.
Product
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-UC-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-UC-0800-52, 0998-00-0800-53, 0998-UC-0800-53, 0998-00-08
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·23V617000·2023-09-05
Peterbilt and Kenworth trucks recalled for fuel hose production defects
Remote Stage 2 fuel filter hoses in 2023-2024 Peterbilt and Kenworth trucks may be damaged, risking disconnection, engine stall, and fuel leaks that could cause fire or crashes.
Product
PETERBILT — 2023 PETERBILT 548
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·23788·2023-08-31
Polaris MATRYX PRO RMK and MATRYX RMK KHAOS Snowmobiles Recalled for Puncture Hazard
Polaris is recalling about 15,900 Model Year 2022–2023 MATRYX PRO RMK and MATRYX RMK KHAOS snowmobiles because handlebar hooks pose a puncture hazard and risk of serious injury during crashes. The firm has received four reports of puncture wounds.
Product
Polaris Snowmobiles, Model Year 2022-2023 MATRYX PRO RMK and MATRYX RMK KHAOS
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·23269·2023-08-31
Frigidaire Gas Cooktops Recalled for Gas Leak and Fire Hazard
Electrolux Group is recalling about 215 Frigidaire gas cooktops because plastic control knobs with black shafts can crack or break during use, creating a risk of gas leak and fire. Electrolux has received 63 reports of cracking or breaking, including one minor injury from a gas leak and one report of fire.
Product
Frigidaire Stainless-Steel 30-inch 4 Burner and 36-inch 5 Burner Gas Cooktops
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·F-1451-2023·2023-08-30
Team Fresh & Go Mixed Fruit Cup Recalled Due to Potential Listeria Contamination
Freshy Foods, LLC is recalling Team Fresh & Go Mixed Fruit Cup due to potential Listeria monocytogenes contamination in 249 units distributed to facilities in Florida, Louisiana, and Mississippi.
Product
Team Fresh & Go: Mixed Fruit Cup, packaged in 16oz plastic cup with lid. Packaged and sold as single unit.
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1481-2023·2023-08-30
Soft Zero on the Go Lite Peanut Butter Ice Cream Recalled for Listeria
Soft Zero on the Go brand Lite Peanut Butter ice cream is being recalled due to potential Listeria monocytogenes contamination. The affected product was distributed across multiple U.S. states and internationally.
Product
Soft Zero on the Go brand Lite Peanut Butter flavor; 8 fl oz; UPC 0-91404-15285-3
Category
Food
Distribution
20 states
SevereFDA (Food)·F-1477-2023·2023-08-30
Soft Serve on the Go Vanilla Chocolate Ice Cream Recalled for Listeria
Real Kosher Ice Cream, Inc. is recalling Soft Serve on the Go brand Vanilla Chocolate ice cream due to potential Listeria monocytogenes contamination. The product was distributed across multiple U.S. states and several countries.
Product
Soft Serve on the Go brand Vanilla Chocolate flavor; 8 fl oz; UPC 0-91404-15129-0 Soft Serve on the Go brand Parve Vanilla Chocolate flavor; 8 fl oz; UPC 0-91404-15113-9
Category
Food
Distribution
20 states
SevereFDA (Food)·F-1450-2023·2023-08-30
Freshy Foods Recalls Team Fresh & Go Cantaloupe Cups for Listeria Risk
Freshy Foods is recalling Team Fresh & Go Cantaloupe Cups due to potential Listeria monocytogenes contamination. The affected product was distributed in Florida, Louisiana, and Mississippi.
Product
Team Fresh & Go: Cantaloupe Cup, packaged in 12oz plastic cup with lid. Packaged and sold as single unit.
Category
Food
Distribution
3 states
SevereFDA (Food)·F-1479-2023·2023-08-30
Soft Serve on the Go Ice Cream Recalled Due to Listeria Contamination
Real Kosher Ice Cream's Soft Serve on the Go Caramel Vanilla ice cream (8 fl oz) may be contaminated with Listeria monocytogenes. The product was distributed across multiple US states and internationally.
Product
Soft Serve on the Go brand Caramel Vanilla flavor; 8 fl oz; UPC 0-91404-15131-3
Category
Food
Distribution
20 states
SevereFDA (Food)·F-1452-2023·2023-08-30
Pineapple Cup Recall Due to Listeria Contamination Risk
Freshy Foods, LLC is recalling Team Fresh & Go Pineapple Cups due to potential Listeria monocytogenes contamination. The recall affects 214 units distributed in Florida, Louisiana, and Mississippi.
Product
Team Fresh & Go: Pineapple Cup, packaged in 12oz plastic cup with lid. Packaged and sold as single unit.
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2248-2023·2023-08-30
Carina Sub-Acute Care Ventilator Recalled for Toxic Chemical Emission
Draeger Medical is recalling 11,621 Carina Sub-Acute Care Ventilators because polyurethane components emit 1,3-Dichloropropan-2-ol at levels exceeding safe limits during extended use in pediatric patients.
Product
Carina Sub-Acute Care Ventilator
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1478-2023·2023-08-30
Soft Serve on the Go Peanut Butter ice cream recalled for Listeria contamination
Real Kosher Ice Cream recalls Soft Serve on the Go Peanut Butter ice cream due to potential Listeria contamination. Consumers should discard the product or return it.
Product
Soft Serve on the Go brand Razzle n' Dazzle Peanut Butter flavor; 8 fl oz; UPC 0-91404-15133-7
Category
Food
Distribution
20 states
SevereFDA (Food)·F-1480-2023·2023-08-30
Soft Serve on the Go Strawberry Mango Sorbet Recalled for Listeria Contamination Risk
Real Kosher Ice Cream, Inc. is recalling Soft Serve on the Go brand Strawberry Mango Sorbet due to potential Listeria monocytogenes contamination. The product was distributed across multiple U.S. states and international locations.
Product
Soft Serve on the Go brand Sorbet Strawberry Mango Sorbet flavor; 8 fl oz; UPC 0-91404-15128-3
Category
Food
Distribution
20 states
SevereNHTSA·23V595000·2023-08-25
2023 Ford F-250 and F-350 Super Duty rear axle shaft defect
Ford is recalling certain 2023 F-250 and F-350 Super Duty vehicles with single rear wheels because the left rear axle shaft may be improperly heat-treated and could break, potentially causing loss of drive power or vehicle rollaway.
Product
FORD — 2023 FORD F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1454-2023·2023-08-23
Black melon seeds recalled for undeclared soy and wheat allergens
Richin Trading Inc is recalling Tim Heung Yuen Black Melon Seed due to undeclared soy and wheat allergens. The product was distributed across 12 U.S. states. Consumers with these allergies should not consume the product.
Product
Tim Heung Yuen Black Melon Seed 6 oz., 12 oz. Ingredients: Melon Seeds, Salt, Sugar & Anise Seed Distributed By Richin Trading Inc. TEL (626) 308-3212 Allergen Warning: This repacked product was processed on shared equipments that also processed peanuts, soybean, and nuts. UPC 7
Category
Food
Distribution
12 states
CriticalFDA (Devices)·Z-2383-2023·2023-08-23
FDA Recalls Dialysis Catheters for Center Lumen Obstruction Risk
Covidien is recalling MAHURKAR dialysis catheters because the center lumen may be blocked by excess silicone lubricant. This could delay treatment and cause blood clots, hemolysis, or embolism.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions REF: 8888345520HP
Category
Medical Device
Distribution
Distributed nationwide

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