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.
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.
Minimum severity
The ANGIOGUARD RX / XP emboli capture guidewire system may separate from its delivery sheath during medical procedures, potentially leading to stroke or complications requiring emergency intervention.
Cordis US Corp is recalling the ANGIOGUARD RX / XP Emboli Capture Guidewire System because the device may separate during procedures, risking stroke or requiring emergency intervention.
Cordis US Corp is recalling ANGIOGUARD RX/XP Emboli Capture Guidewire Systems worldwide due to potential separation of the delivery system and capture sheath during procedures, which could cause stroke or require emergency intervention.
Cordis is recalling an emboli capture guidewire system due to potential separation of components during medical procedures. The separation could cause procedural delays, unplanned interventions, or stroke.
Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Trays because the device connectors are not making secure connections with 15mm caps and other circuit components, resulting in unsecure connections.
Fresh From Meijer Shareable Garden Salad 11.5 oz is being recalled due to potential Listeria monocytogenes contamination. The recall affects salads distributed to Meijer stores across six states with a sell-by date of 3/31/2023.
Meijer Inc is recalling Fresh From Meijer Mediterranean Salad due to potential Listeria monocytogenes contamination. Approximately 1,064 units were distributed to Meijer stores in six Midwest states.
Camber Pharmaceuticals is recalling Atovaquone Oral Suspension due to contamination by Bacillus cereus bacteria. The contamination was discovered during testing of repackaged medication.
The ANGIOGUARD RX/XP Emboli Capture Guidewire System may separate from its delivery sheath during medical procedures, potentially causing stroke or requiring emergency surgery. Cordis US Corp is recalling 146 units worldwide.
Cordis US Corp is recalling the ANGIOGUARD RX/XP Emboli Capture Guidewire System (1,087 units worldwide) due to potential separation of the delivery system and capture sheath, which could lead to stroke.
Daiso California Warehouse is recalling Kimura burdock salt because it contains fish (sardines, bonito, tuna) not listed on the label. People with fish allergies may have a serious allergic reaction.
Meijer is recalling Fresh From Meijer Tomato Caprese Salad due to potential Listeria monocytogenes contamination. The product was distributed to stores across six states.
Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Sets due to unsecure connections with 15mm caps and circuit components that may disconnect during medical procedures.
ANGIOGUARD RX/XP emboli capture guidewire systems may separate from their delivery sheaths during interventional procedures, potentially causing stroke. Cordis is recalling 56 units distributed worldwide.
Cordis US Corp recalls 54 units of the ANGIOGUARD RX/XP Emboli Capture Guidewire System due to potential separation of device components. This could delay procedures or result in unplanned intervention, including possible stroke.
Ford is recalling certain 2023 F-250, F-350, and F-450 Super Duty vehicles due to loose or missing steering column bolts that could cause steering column separation, increasing the risk of crashes due to loss of steering control.
Peloton is recalling approximately 2.2 million Model PL01 exercise bikes because the seat post assembly can break during use, causing users to fall. The company has received 35 reports of seat post breakage, including 13 reports of injuries such as fractured wrists, lacerations, and bruises.
BRP U.S. Inc. is recalling about 12,500 Ski-Doo snowmobiles from model years 2021 and 2022 because a fuel injector hose retainer screw can loosen, cause fuel leaks, and pose a fire hazard. Four fires have been reported.
The FDA recalls NUX Male Enhancement capsules distributed nationwide because they contain undeclared sildenafil and tadalafil, making them an unapproved drug. Consumers should not use this product.
Jabsons Foods is recalling Thai sweet Chilli Roasted Peanut due to undeclared milk. The recall affects 508 cases distributed domestically in the United States.
Salento Organics is recalling Dark Chocolate Goldenberry Bites due to undeclared milk. The product poses a serious risk to consumers with milk allergies.
Salento Organics Dark Chocolate Mango Bites are recalled due to undeclared milk, which poses a risk to consumers with milk allergies.
Jabsons Foods has voluntarily recalled Tandoori Kaju Cashew Nuts because the product contains undeclared milk, a common allergen. This is a Class I recall affecting consumers with milk allergies.
Tandoori Roasted Peanuts in 4.94 oz pouches are recalled due to undeclared milk. Consumers with milk allergies should not consume the product.
Salento Organics is recalling Dark Chocolate Banana Bites due to undeclared milk content, a major allergen. The recall affects multiple lot numbers distributed domestically and internationally.