Severity 4 of 5
The hazard poses a serious risk of illness, injury, or structural failure. 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.
McNeilus is recalling 19 model year 2016 Bridgemaster V Concrete Mixers because bridge axle tube sleeves may crack, potentially causing the axle to detach and increasing crash risk.
Hendrickson is recalling specific bridge axles manufactured in late 2015 and early 2016 because tube sleeves may crack, potentially causing the axle to detach from the vehicle.
Maserati is recalling 2014 Quattroporte and Ghibli vehicles because the gear indicator may mislead drivers about the transmission position, creating a risk of injury when exiting.
PACCAR is recalling 2017 Kenworth and Peterbilt trucks because a defective engine control module may cause the engine to stall without warning, increasing crash risk.
Vermeer is recalling 2014-2016 TG5000 Tub Grinder trailers because incorrectly installed spherical washers may cause the kingpin to detach, increasing crash risk.
Honda is recalling specific 2015-2016 Odyssey, Acura MDX, and Pilot vehicles because fuel tank welds may separate, causing a leak that could lead to a fire.
Daimler Trucks is recalling 2008-2009 Sterling Bullet 4500 and 5500 chassis cabs because passenger air bag inflators may rupture, posing a risk of serious injury or death.
Integra LifeSciences is recalling 2,487 MicroFrance electrosurgical instruments due to reports of unintended patient or operator burns and electric shock.
World's Choice Products is recalling Supreme Elixir 32oz. bottles due to undeclared whey protein containing milk and soy lecithin.
Akorn, Inc. is recalling specific lots of Sulfacetamide Sodium Ophthalmic Solution because they failed antimicrobial effectiveness testing, raising concerns about sterility.
Invisiblu International LLC is recalling LGD-Xtreme capsules containing unapproved ligandrol because the product was marketed without an approved NDA or ANDA.
Baptist Health Medical Towers Pharmacy is recalling seven bags of TPN 1 (amino acid 20%) in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 88 bags of Vancomycin 1500 mg in 270 mL 0.9% NS due to a lack of sterility assurance.
FDA is recalling Curity All Purpose Sponges due to compromised sterility from a barrier breach. The recall affects units distributed in the US and 20 other countries.
Frank L Harter & Sons Inc. is recalling 548 cases of 5 lb pasta salad containers because the labels failed to list milk and soy as ingredients.
Covidien LLC is recalling Vistec X-Ray Detectable Sponges because a breach of the barrier packaging may have compromised sterility.
Baptist Health Medical Towers Pharmacy is recalling 47 bags of Vancomycin 750 mg in 250 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling seven bags of Nafcillin 3 grams in 277 mL 0.9% NS due to a lack of sterility assurance. The product was distributed in Arkansas.
Giant Eagle is recalling Walnut Delights 6 Packs because the labels fail to declare the milk ingredient and allergen.
World's Choice Products is recalling Xtreme Fiber Detox because it contains undeclared whey protein (milk) and soy lecithin.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
Baptist Health Medical Towers Pharmacy is recalling 54 bags of Vancomycin 1750 mg in 270 mL 0.9% NS due to a lack of sterility assurance. The product was distributed in Arkansas.
Covidien LLC is recalling Curity Gauze Sponges because a breach of the barrier packaging may have compromised their sterility.
Baptist Health Medical Towers Pharmacy is recalling 14 bags of Daptomycin 650 mg in 50 mL 0.9% NS due to a lack of sterility assurance.
Giant Eagle is recalling Pecan Tassies because the ingredient and allergen statements fail to declare milk. This poses a risk to consumers with milk allergies.