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.
PACCAR is recalling 2025 Kenworth T880 and other commercial vehicles due to steering arm and tie rod bracket fasteners that may fail, resulting in loss of steering control and increased crash risk.
Volvo is recalling 2019-2024 VN and VHD trucks because passenger side bench seats may be inadequately attached to the floor. If the seat attachment fails during a crash, the seat could shift, increasing the risk of injury.
Winnebago Industries is recalling 2025 Navion and View motorhomes because a screw may damage the seat belt retractor. A damaged retractor may not secure occupants properly, increasing the risk of crash-related injury.
Certain 2025 Freightliner and Western Star commercial vehicles may have improperly heat-treated tie rod assemblies that can fail, potentially causing loss of steering control and increasing crash risk.
Medtronic Duet External Drainage System catheters may disconnect from stopcocks, potentially compromising cerebrospinal fluid management. The FDA Class I recall affects 3,889 units distributed worldwide.
Medline Industries is recalling IV securement kits and neonatal PICC line insertion trays due to potential lack of sterility in Nurse Assist components. Approximately 11,812 units are affected.
Vyaire Medical is recalling 106,656 units of AirLife Adult Manual Resuscitator bags due to faulty components that may break during use, causing ventilation failure and potentially leading to hypoxia or death.
Sargento Foods is recalling Sargento Deep V Shredded Taco Cheese Blend (UPC 46100352281) due to potential Listeria monocytogenes contamination. The recall affects 956 cases distributed across 15 states.
Medline Industries is recalling certain medical kits and trays that may contain non-sterile solutions. Healthcare facilities should discontinue use of affected batches to prevent patient exposure to potential contamination.
Medline Industries is recalling certain dialysis kits and trays due to potential sterility defects in component irrigation solutions and saline products. Non-sterile solutions used in dialysis could cause infection.
Honda recalls 2023 Civic vehicles with a defective brake modulator that may leak fluid, potentially causing unintended vehicle movement or increased brake pedal travel.
Sargento Fancy Shredded Italian Cheese Blend is recalled for potential Listeria monocytogenes contamination. 97 cases were distributed across 15 states.
Medline Industries is recalling 228 medical device trays due to potential sterility defects in component solutions used in medical procedures.
Medline is recalling 1,270 prep kits containing components that may lack sterility. Solutions from Nurse Assist used in the kits may not be sterile.
Lakeview Farms LLC is recalling Rojo Black Bean 6 Layer Dip due to potential Listeria monocytogenes contamination. Consumers should not consume the product and should discard or return it.
Medline Industries is recalling 14,234 units of Centurion surgical kits and trays that may contain non-sterile irrigation solutions. The affected products were manufactured using compromised Nurse Assist components.
Sargento Foods is recalling White Cheddar cheese products due to Listeria monocytogenes. The affected products were distributed in 15 states; consumers should discard them.
Medline Industries is recalling Centurion maintenance flush and blood draw kits that may lack sterility due to defective components, potentially allowing infections during medical procedures.
Medline Industries is recalling 139 surgical kits containing irrigation solutions with potential sterility issues. The recalled products were distributed nationwide and internationally.
Medtronic is recalling 30,711 units of its Duet External Drainage System because of the potential for catheter disconnection from patient line stopcock connectors.
Ready Pac Foods is recalling Marketside Southwest Chopped Kit (10.3 oz.) due to potential Listeria monocytogenes contamination. Consumers should not consume the affected product.
Medline Industries is recalling certain sterile medical kits and trays that contain component solutions with a potential lack of sterility. Non-sterile solutions could result in infection or contamination during medical procedures.
Medline Industries is recalling 26,171 kits and trays containing potentially non-sterile irrigation solutions and syringes supplied by Nurse Assist, which could pose risks if used in medical procedures.
Medline Industries is recalling approximately 2,205 wound irrigation kits due to potential lack of sterility in component solutions. Non-sterile irrigation solutions pose a risk of infection during wound care.
Vyaire Medical is recalling approximately 1.8 million AirLife Adult Manual Resuscitators worldwide due to faulty molded components that may fail to deliver proper ventilation, risking hypoventilation and hypoxia.