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.
Minimum severity
About 320 Urban Arrow FamilyNext Pro cargo e-bikes sold between March and December 2025 are being recalled because the cargo area buckle can fail to latch, posing injury risks to children.
Northern Tool + Equipment is recalling about 1,416 NorthStar hot water pressure washers because the fan wheel can fail, causing abnormal burner operation that produces smoke and bursts of flames. No injuries have been reported.
Starmatrix Group is recalling about 2,390 Sunneday and Blue Bay above-ground pools (48+ inches) because a compression strap creates a foothold allowing unsupervised child access, posing a drowning risk. No injuries have been reported.
Bazic Products is recalling Bazic Silicone Glue due to methanol poisoning risk. The packaging is not child-resistant as required by law, and the product is incorrectly labeled as non-toxic.
Mindbodygreen recalled approximately 148,370 Ultimate Multivitamin+ bottles for non-compliance with child-resistant packaging requirements. The iron-containing supplements pose a risk of serious injury or death if swallowed by young children.
Gregory's Foods is recalling its White Chocolate Macadamia Nut frozen cookie dough due to undeclared peanuts. The product was distributed in Minnesota, North Dakota, Nebraska, and Wisconsin.
Medline Industries is recalling Full Electric Lightweight Homecare Beds due to a fire hazard in the hand control pendant. The pendant may overheat under certain operating conditions and pose a risk of fire.
Medline is recalling Full Electric Basic Homecare Beds because the hand control pendant may overheat and catch fire in rare scenarios. The company has received 58 complaints of pendant sparking, burning, melting, or fire.
Anthony's Barbecue & Dip-It Sauce contains an undeclared fish allergen (anchovy from Worcestershire). The product poses a serious risk to consumers with fish allergies.
White Castle Original Sliders may contain undeclared milk and soy allergens. Approximately 1,021 cases distributed to Illinois, Ohio, and Texas with best-by date April 18, 2026.
Medline is recalling 373,392 Semi Electric Basic Homecare Beds due to hand control pendants that may overheat and pose a fire risk. The company has received 58 complaints of pendant sparking, burning, melting, and smoking.
Medline Industries recalls homecare beds due to fire risk in the hand control pendant. The pendant may overheat and ignite, posing a fire hazard to users.
Medline is recalling Full Electric Low Basic Homecare Beds due to a fire hazard in the hand control pendant. The pendant may overheat under certain operating conditions, creating a risk of fire.
Medline is recalling 13,245 Semi Electric Lightweight Homecare Beds because hand control pendants may overheat and pose a fire risk in certain conditions. The company has received 58 reports of pendant sparking, burning, melting, smoking, or fire.
ICU Medical Plum Duo infusion pumps have a software issue preventing clinicians from programming the automatic flush feature after piggyback therapy, affecting this critical safety function.
ICU Medical Plum Solo Precision IV pumps may display error messages preventing clinicians from programming the automatic downstream line flush after piggyback therapy.
Merit Medical Systems is recalling 328,000 units of the Allwell Angioplasty Pack because the inflation device handle may detach from the syringe during procedure.
Edan Diagnostics is recalling the EDAN Central Monitoring System due to potential cybersecurity issues identified by the FDA. The system manages information from EDAN medical devices.
A software update to Philips Patient Information Center iX modifies Mobile Event Notification filter settings without alerting users during upgrade. This could result in missed critical patient alerts to medical staff.
Edan Diagnostics is recalling EDAN patient monitors (X8, X10, X12 models) due to potential cybersecurity issues identified in an FDA letter. Approximately 3,824 units were distributed worldwide.
RayStation/RayPlan radiation therapy treatment planning software contains a defect where dose calculation invalidation may fail for certain treatment areas, potentially affecting treatment planning accuracy.
Merit Medical is recalling Custom Manifold Kits (REF: K09-13203A) due to a hazard where the inflation device handle may detach from the syringe during procedures. Approximately 2,192 units were distributed worldwide.
Tyber Medical is recalling 64 units of VOLT Wrist Treatment System orthopedic plates due to incorrect thread orientation that may affect proper device fixation during surgical repair.
RayStation radiation therapy software versions 11.0.0-11.0.4 fails to recalculate doses when certain regions of interest are modified. The dose invalidation function does not work properly for ROIs without contours that have material overrides or are type Bolus, Fixation, or Support.
EDAN Vital Signs Monitor iM3 models are being recalled due to potential cybersecurity vulnerabilities identified in an FDA letter. Approximately 11,987 units were distributed nationwide and in Mexico.