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 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.
Minimum severity
GE Healthcare CARESTATION 750c A1 anesthesia systems may not provide effective ventilation in Volume Control Ventilation mode. Affected units can achieve ventilation through alternative modes or manual operation.
GE Healthcare CARESTATION 620 A1 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Effective ventilation is available in Pressure Control or Manual ventilation modes.
Certain GE Healthcare Carestation anesthesia delivery systems may fail to provide effective ventilation in Volume Control Ventilation (VCV) mode. Affected systems can still be used safely in Pressure Control Ventilation or Manual ventilation modes.
GE Healthcare is recalling certain CARESTATION anesthesia systems that may fail to provide effective ventilation in Volume Control Ventilation mode. Alternative ventilation modes remain functional.
Hyundai is recalling certain 2025 Palisade vehicles because an insufficient seal on the electric oil pump controller can allow moisture to accumulate and cause an electrical short that may result in fire. Owners should park vehicles outside and away from structures until the repair is completed.
Prevost is recalling one 2025 X3-45 VIP Entertainer because front lower control arm fasteners may be improperly tightened, risking vehicle control loss.
Ferrarini USA is recalling approximately 70 pounds of ready-to-eat sliced prosciutto imported without required reinspection. No illnesses have been reported.
Tiffin is recalling 2025 Zephyr motorhomes because the secondary emergency exit is on the same side as the primary exit, increasing injury risk.
Baseus 65W 30000mAh portable chargers (model BS-30KP365) are being recalled because the lithium-ion battery can overheat and catch fire. The manufacturer has received 76 reports of incidents, including 4 fires and 3 reports of property damage.
SharkNinja is recalling about 1.8 million Foodi OP300 Series pressure cookers because the pressure-cooking lid can open during use, causing hot contents to escape and burn injuries. The company has received 106 reports of burn injuries, including more than 50 second- or third-degree burns.
Walker's Wine Juice Pumpkin Juice in 2.5, 5, 30, 60, and 275 gallon bulk containers is being recalled due to potential contamination with Clostridium botulinum. The product was distributed across multiple states.
MO-CHA brand Premium Non-Dairy Creamer is recalled because the label does not declare milk as an allergen, despite milk being present in the product. Consumers with milk allergies are at risk of adverse reaction.
Abbott is recalling the Amplatzer TorqVue LP Catheter (Model 9-TVLPC4F90/080) due to a potential small breach in the proximal shaft that may not be visible and could lead to prolonged procedures, blood loss, or air embolism.
Zaarah Herbals brand Gurmar Powder is being recalled due to elevated lead levels. The product was distributed in New York, Connecticut, New Jersey, and California.
Zaarah Herbals brand Rasayan Churan (100g jars) is recalled due to elevated lead levels of 88.038 ppm. The product was distributed in New York, Connecticut, New Jersey, and California.
Denver Solutions, LLC DBA Leiters Health is recalling PHENYLephrine HCl 0.5 mg per 5mL single-dose syringes because some syringes may be leaking or damaged, which could compromise sterility assurance.
Denver Solutions, LLC DBA Leiters Health is recalling Rocuronium Bromide 50 mg per 5mL syringes due to potential leaking or damage that may compromise sterility assurance.
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection vials nationwide because some media fill units showed bacterial contamination, indicating a lack of sterility assurance. The affected product is a 100mg/mL injectable antipsychotic medication.
Zaarah Herbals brand Bhringraj Powder contains elevated levels of lead and arsenic. Consumers should not use the product and should contact the recalling firm for instructions.
Leiters Health is recalling dexmedetomidine HCl PF syringes nationwide due to leaking or damaged syringes that may not maintain sterility. Affected lot 2431276A has an expiration date of 4/20/2025.
Conavi Medical Inc. is recalling the Novasight Hybrid Catheter (Model TA-06-0001) due to manufacturing issues that could cause the catheter sheath to detach. The device is used for diagnostic intravascular imaging.
Cromer Food Services is recalling chicken salad sandwiches because milk was not declared on the label. Consumers with milk allergies are at risk.
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility and bacterial contamination detected in some media fill units. The affected product was distributed nationwide.
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility and bacterial contamination detected in some media fill units. The drug is used for intramuscular injection to treat psychiatric conditions.
Denver Solutions, LLC is recalling Ketamine HCl 50mg per 5mL single-dose syringes nationwide due to leaking or damaged syringes that may lack sterility assurance. Two affected lots are identified with expiration dates in July 2025.