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
Danisco USA Inc. recalls Grindsted Sour Cream 6563 stabilizer system for potential Salmonella contamination affecting 33,600 kg distributed across the US, Canada, and Mexico.
Hormel Foods is recalling Planters Deluxe Lightly Salted Mixed Nuts (8.75 oz) due to possible Listeria monocytogenes contamination. The recall affects 6,804 cans distributed to five southeastern states.
Danisco USA Inc. recalls Grindsted Turkey Hill 1512 NF NSA Stabilizer and Emulsifier System (10 lot numbers) due to potential Salmonella contamination. The 2,270-pound product was distributed to 28 US states, Canada, and Mexico.
Arrow International is recalling intra-aortic balloon catheter kits due to potential inflation failure, catheter damage, and helium loss that could cause serious health consequences.
Danisco USA Inc. is recalling Grindsted Creamer 2103 Stabilizer and Emulsifier System due to potential Salmonella contamination. Approximately 36,265 kg was distributed across multiple U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Iced Coffee 6752 Stabilizer System in 50 lb bags due to potential Salmonella contamination. The recall affects product distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Avicel-plus GP 1615 Stabilizer System FCC due to potential Salmonella contamination. The affected bulk food additive was distributed to manufacturers across multiple U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Germantown Enhance Plus Stabilizer System (lot 1204572178) due to potential Salmonella contamination. The product was distributed across multiple US states, Canada, and Mexico.
Multiple brands of yogurt pretzels are being recalled due to potential Salmonella contamination. Affected products were distributed in California and Washington.
Danisco USA Inc. is recalling Grindsted Creamer 1817 Stabilizer System due to potential Salmonella contamination. The product was distributed to 23 U.S. states, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted Creamer 2160 System bags due to potential Salmonella contamination. The recall affects 31,865.40 kg distributed across the US, Canada, and Mexico.
Danisco USA Inc. is recalling Grindsted SSD 6018 Stabilizer System due to potential Salmonella contamination. The product has been distributed to customers in the United States, Canada, and Mexico.
Arrow International is recalling its UltraFlex Intra-Aortic Balloon Catheter Kit because of infrequent device malfunction that could lead to serious health consequences. 44,807 units are affected worldwide.
PJ TRAILERS is recalling certain 2024-2025 LD trailers because air ride suspension brake axles may be installed incorrectly. This could reduce braking ability and increase the risk of crashes.
Keystone RV is recalling 2021-2022 Crossroads Redwood, Dutchmen Voltage, and Yukon trailers for improperly tightened axle U-bolts that may cause loss of vehicle control and crash risk.
Good Earth Lighting is recalling more than 1.2 million rechargeable integrated lights whose lithium-ion batteries can overheat and ignite the plastic housing, posing fire and burn hazards. One death has been reported.
Kawasaki is recalling approximately 68,500 engines used in lawn and garden equipment from multiple brands due to overheating that can cause fire and burn hazards. Consumers should stop using affected equipment and contact the manufacturer or an authorized dealer for free repair.
Medline endotracheal tubes with subglottic suctioning may have inflation tubes that detach or tear and suction pumps that disconnect, risking loss of ventilation control.
Gibson Farms Organic Nuts – Light Halves and Pieces are recalled due to potential E. coli O157:H7 contamination. Affected lots 3325-043 and 3341-501 were distributed to California and Washington.
Revive Rx Pharmacy recalls 751 vials of compounded tirzepatide (Lot #748127) labeled to contain tirzepatide but actually filled with testosterone cypionate. Patients receiving this medication may take the wrong drug with serious health consequences.
Hy-Vee Stores Inc is recalling Hy-Vee To Go and Hy-Vee Cookies & Cream Mix products due to potential Salmonella contamination. Affected products were distributed in eight Midwest states.
Medline is recalling about 1.5 million Bed Assist Bar adult bed rails because users can become entrapped between the rail and mattress, posing a risk of asphyxiation. Two deaths have been reported.
Hikma Injectables USA Inc is recalling phenylephrine injection syringes that were mislabeled as containing ephedrine. The mix-up creates a serious risk of administering the wrong medication to patients.
Sammy's Milk Goat Milk Toddler Formula is recalled because the manufacturer made false claims it was safe for infants as a sole nutrition source. The product lacks FDA premarket approval and does not meet infant formula manufacturing standards.
Philips BiPAP V30 Auto Ventilators may interrupt or lose therapy during a Ventilator Inoperative alarm, potentially causing hypoventilation, severe oxygen depletion, or respiratory failure.