Severity 4 of 5
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Crenlux pool drain covers violate federal safety standards and pose risks of entrapment and drowning. About 200 units sold on Amazon from June 2025 through March 2026 are affected.
Vornado is recalling about 255,000 SRTH small room tower heaters because the fan blade can detach, causing overheating and fire. Vornado has received 32 overheating reports, including eight fires and one smoke inhalation.
Legacy Bakehouse LLC is recalling Butter Parsley Bagel Crisps due to Salmonella contamination from recalled milk powder. The affected products were distributed in Pennsylvania and Wisconsin.
Giant Eagle Baked Pita Chips with Parmesan, Garlic & Herb and Bagel Crisps are recalled due to Salmonella contamination from California Dairies milk powder. The affected products were distributed in Pennsylvania and Wisconsin.
Parmesan & Herb Bagel Crisps from Legacy Bakehouse LLC are being recalled due to Salmonella contamination from a recalled milk powder ingredient. Affected product was distributed in Pennsylvania and Wisconsin.
Medline is recalling spinal anesthesia kits containing Huons bupivacaine hydrochloride due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints. Affected kits were distributed worldwide.
Medline Industries is recalling 41,720 spinal anesthesia trays containing Bupivacaine due to quality issues, microbiology testing data integrity concerns, and reported efficacy complaints affecting patient safety.
Medline Industries recalled approximately 28,106 anesthesia kits containing Huons bupivacaine due to microbiology testing data integrity concerns and reported efficacy complaints.
Abiomed is recalling 91 Automated Impella Controllers due to hardware defects that could interrupt motor controls or cause pump failure in this cardiac support device.
Wawa is recalling Diet Iced Tea Lemon in 16oz bottles due to undeclared milk allergen that may affect consumers with milk allergies. Bottles were distributed across five states.
Honeyville, Inc. is recalling a bulk banana smoothie product due to potential Salmonella contamination from an ingredient used in manufacturing. Distribution was to California and Utah.
Medline Industries recalls 30,120 spinal injection kits containing Huons Bupivacaine due to quality control failures and reported efficacy complaints. The FDA Class I recall affects kits distributed in the US and selected territories.
Medline is recalling 1100 anesthesia trays containing Bupivacaine due to quality issues, microbiology testing data integrity concerns, and reported efficacy complaints. The kits were distributed worldwide to healthcare facilities.
Bolton Medical's RelayPro Thoracic Stent-Graft System may fail to release from its delivery system due to proximal clasp disconnection. This FDA Class I recall affects multiple device configurations distributed worldwide.
Wawa Iced Tea Lemon 16 oz bottles are recalled due to undeclared milk allergen. The product was distributed in Delaware, Maryland, New Jersey, Pennsylvania, and Virginia.
Abiomed is recalling 625 units of the Automated Impella Controller due to alarm failures, electrical faults, and mechanical misalignment that may prevent proper device function.
Wawa Beverage Company is recalling Wawa Fruit Punch Pint (16oz) bottles due to undeclared milk allergen. The product was distributed to Delaware, Maryland, New Jersey, Pennsylvania, and Virginia.
Volvo Trucks is recalling certain 2023-2025 VN trucks because their brakes may take longer than expected to activate, increasing the stopping distance and crash risk. Dealers will install a new pneumatic circuit.
Shyft Group is recalling approximately 797 Spartan K2, K3, and K4 RV chassis from 2023-2025 due to foreign material in the steering gear that may cause loss of power steering assist, increasing crash risk.
Synear Foods USA is recalling approximately 71,603 pounds of frozen pork and crab soup dumplings due to undeclared peanut allergen in the product. The products were distributed in California, New Jersey, and Washington; consumers should not consume them.
Giantex outdoor lounge chairs model NP10025NY pose an amputation risk when adjusting the backrest due to exposed pinch points. One finger amputation has been reported.
Walmart is recalling about 165,000 Mainstays 9-Drawer Fabric Dressers because they can tip over and cause entrapment if not anchored to a wall, creating a risk of serious injury or death to children.
Joy Furniture is recalling about 10,400 Talan and Royce sofas, loveseats, and recliners due to a fire hazard in the power switch that can overheat. The firm has reported 41 incidents including smoking, burning, and two fires, with no injuries reported so far.
Giantex and Costway portable steam saunas are recalled because the steam diffuser can position too close to the user's body, causing burns. Giantex has received nine burn reports, including one second-degree burn.
Missry Associates recalls Misco Sports Light-Up Racket Sets (model MT2287) because the battery compartment screw can detach and button cell batteries in the shuttlecock can be easily accessed by children, posing risk of serious injury or death if swallowed.