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.
Ventec Life Systems is recalling VOCSN V+Pro ventilator units because they may not have been fully tested for high-pressure conditions, which could cause oxygen leaks and increase fire risk during use.
Fresenius Medical Care is recalling DELFLEX Dextrose Peritoneal Dialysis Solution bags due to potential leaks from bag perforations that could compromise sterility. Affected patients should contact their healthcare provider immediately.
CareFusion 213, LLC is recalling BD PurPrep (povidone-iodine 8.3% with isopropyl alcohol 72.5%) due to lack of assurance of sterility and potential product contamination. Affected lots are distributed nationwide.
AVID Medical is recalling Halyard CARDIAC CATH PACK SAN23CARDQ kits (Model DRCC36) due to a Medline syringe rotating adapter that may unwind during use, potentially causing loose or full disconnection between the syringe and manifold.
Erbe Medical is recalling ERBEFLO CleverCap CO2 hybrid tubing and cap sets used with endoscopes because the distal connector may allow unintended water flow, potentially leading to water aspiration and serious respiratory complications.
AVID Medical recalls Halyard Cardiac Cath Pack kits (Models EAMC1000-05, WAFB208-02) due to risk that a Medline syringe rotating adapter may unwind during use, causing loose or full disconnection between the syringe and manifold.
Medline Industries is recalling six models of medical device convenience kits due to calibration issues with sterilization and packaging equipment that may have reduced sterility assurance levels. The recall affects 553 units distributed nationwide.
AVID Medical is recalling the Halyard HEART CATH SELF REGIONAL kit (Model SELF131-05) because the Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.
Medical Action Industries is recalling Pack Cath BHH catheter kits because the rotating adapter may unwind during use, causing a loose or full disconnection between the syringe and manifold.
The Halyard PERC TRAY kit (models SLPC34-01 and SLPC34-02) is being recalled due to risk that a Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.
Erbe Medical is recalling ERBEFLO 2 Endoscopy Pump Tubing/Cap Sets due to a connector design that may allow unintended water flow, potentially leading to water aspiration and serious respiratory conditions.
California Dairies Inc. is recalling over 1.1 million pounds of Low Heat Non-Fat Dried Milk Powder due to potential Salmonella contamination. The product was distributed in the US and to Mexico, Philippines, and Dominican Republic.
California Dairies Inc. is recalling Low Heat Non-Fat Dried Milk Powder due to potential Salmonella contamination. Affected batches were produced between August and November 2025 and distributed in the United States and internationally.
Givaudan Flavors Corp is recalling bulk WN-976-782-1 Seasoning for Cheese Sauce due to potential Salmonella contamination. The product was distributed as a bulk ingredient in 43.50-lb. bags.
Griffith Foods Inc. is recalling MILK-N-EGG MIX (50-pound bags) due to potential Salmonella contamination in the nonfat dry milk component. The product was distributed to 15 states.
Raw Farm LLC is recalling raw cheddar cheese due to a multi-state outbreak of E. coli O157:H7. Affected consumers should not consume the product and should discard it or return it to the retailer.
Raw Farm shredded raw cheddar cheese is being recalled due to a multi-state E. coli O157:H7 outbreak. The product was distributed to consumers across multiple U.S. states.
Griffith Foods is recalling nonfat dry milk (Milk Wash) sold to Chick-fil-A due to potential Salmonella contamination. The product was distributed across 15 states.
American Contract Systems is recalling 7,311 convenience kits containing Medline angiographic control syringes. The rotating adaptor may unwind during use, potentially causing disconnection and risks including blood loss, infection, and air embolism.
California Dairies Inc. is recalling buttermilk powder due to potential Salmonella contamination. The affected product was distributed in the United States and to Mexico, Philippines, and Dominican Republic.
Raw Farm Original Raw Cheddar (80 oz bulk) is being recalled due to a multi-state E. coli O157:H7 outbreak. Consumers should not consume this product and should discard or return it.
Toyota is recalling certain 2024-2025 Highlander and Highlander Hybrid vehicles because the third row center seat belt roof anchor may have been installed at an incorrect angle, preventing proper occupant restraint during a crash.
Rollx Vans is recalling wheelchair restraints in multiple vehicle models because retractors may fail to lock. An unsecured wheelchair can move during transit, posing a safety risk.
Plains Meat Co. is recalling 58,400 lbs of fresh and frozen ground beef after E.coli O157:H7 was found during USDA testing.
Kia is recalling 250,547 2021–2024 K5 vehicles due to a faulty check valve in the fuel system. The defect allows air into the fuel tank, causing it to expand, contact hot exhaust components, melt, and create a fire risk.