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.
Zydus Pharmaceuticals is recalling 44,800 bottles of 30mg Paroxetine tablets because foreign Risperidone tablets were found in the packaging.
The Harvard Drug Group is voluntarily recalling Rugby Ferrous Sulfate Liquid due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Monster Energy Company is recalling Java Monster Loco Moca Coffee & Energy because the product was distributed without undergoing the required retort step.
Bella Pharmaceuticals is recalling 7 vials of Methylcobalamin 10mg due to a lack of assurance of sterility. The product was distributed nationwide in the United States.
Leader Liquid Vitamin D Supplement for Breastfed Infants is being voluntarily recalled due to possible contamination with B. cepacia, which may cause serious infections in vulnerable patients.
Bella Pharmaceuticals is recalling Magnesium Chloride 200mg vials because the company cannot ensure the product is sterile.
Bella Pharmaceuticals is recalling specific lots of Calcium chloride 10% vials because the company cannot ensure the product is sterile.
The Harvard Drug Group is voluntarily recalling Rugby Cerovite Liquid due to possible B. cepacia contamination, which may cause serious infections in vulnerable patients.
The Harvard Drug Group is voluntarily recalling Rugby D 3 Vitamin Liquid due to possible B. cepacia contamination, which poses a serious infection risk to vulnerable patients.
Porsche is recalling specific 2003-2006 Cayenne models because a fuel pump flange may crack, allowing fuel to leak and increasing fire risk.
Bella Pharmaceuticals is recalling specific lots of L-Glutamine 100mg vials because the company cannot guarantee the product is sterile.
German Sausage Haus is recalling approximately 1,252 pounds of frozen meat products due to a possible processing deviation that may have led to staphylococcal enterotoxin contamination.
Curt Manufacturing is recalling Class 1 trailer hitches for 2016-2018 Mini Clubman and Countryman vehicles because the mounting points may be inadequate, causing the hitch to sag or separate.
Nissan is recalling 2017 Infiniti Q50 and Q50 Hybrid vehicles because the driver's air bag inflator may be improperly welded, increasing injury risk in a crash.
Forest River is recalling 2015-2018 Vibe and 2016-2018 Rainier recreational trailers because the liquid propane line may have insufficient clearance, posing a fire risk.
Southwire is recalling Moonrays mystic globe and snow globe stake lights because light refraction can singe or melt nearby items, posing a fire hazard.
Mitsubishi is recalling 2004-2006 Lancer and 2004 Lancer Sportback vehicles because the passenger air bag inflator may rupture in a crash, potentially causing serious injury or death.
Volvo Bus is recalling 2017-2018 Prevost 9700 transit buses because the accelerator pedal may not react when pushed, increasing crash risk.
Diono is recalling specific Radian, Olympia, Pacifica, and Rainier car seats manufactured between late 2013 and early 2017. The seats may not adequately protect children from chest injuries in crashes if installed forward-facing with only a lap belt.
Pierce Manufacturing is recalling 2015-2016 Arrow XT, Enforcer, Impel, Quantum, Saber, and Velocity vehicles because a steering axle nut may not be properly torqued, risking loss of steering.
Kimble Mixer is recalling one 2014 Mixer Custom Chassis because improperly torqued hex nuts on the drive axle could cause the driveshaft to disconnect, increasing crash risk.
Halcore Group is recalling 2016-2017 AEV Traumahawk ambulances because door striker bolts may fail under load, potentially allowing doors to open in a crash.
Cruiser RV is recalling 2018 Shadow Cruiser Ultra Lite trailers because rear axles were installed backwards, potentially reducing braking ability or causing brakes to lock up.
Maquet Datascope is recalling 14,547 CS 100 Intra-Aortic Balloon Pumps worldwide due to a defect that could prevent therapy initiation or continuation.
Southeastern Mills is recalling Shore Lunch Fish Breading Batter Mix because raw buttermilk solids may be contaminated with Salmonella.