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.
New England Natural Bakers is recalling Organic Muesli due to potential Listeria monocytogenes contamination. Consumers should check their pantry for the affected product.
PharMEDium Services is recalling specific lots of Potassium Phosphate in 5% Dextrose Injection due to a media fill failure that compromised sterility assurance.
Lakota is recalling 2017-2018 trailers because the rear external load ramp may detach, creating a road hazard.
Polaris is recalling 16,800 RZR 170 recreational off-highway vehicles because fuel tank necks can crack or wiring can overheat, posing fire risks.
Ford is recalling 94,605 vehicles because improperly manufactured bolts may fracture, increasing injury risk in a crash.
Piaggio is recalling 2018 Liberty 50 iGet 3V scooters because a rear swing arm nut may loosen, potentially causing a loss of control and crash.
Piaggio is recalling 2014-2017 Fly 150 3V scooters because front brake disc mounting screws may loosen, potentially causing the front wheel to lock up and increasing crash risk.
Toyota is recalling 2016 Camry and Avalon Hybrid vehicles because the front drive shaft may separate, potentially causing a loss of propulsion or vehicle roll.
Cesina Sausage Company is recalling 10 pounds of pork kolbassi labeled as ready-to-eat but actually not ready-to-eat. No illnesses have been reported.
Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate Injection due to a lack of assurance of sterility. The product was distributed nationwide.
Wildway LLC is recalling 434 cases of Banana Nut Grain-free Granola due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Polaris is recalling about 25,600 model year 2014 Sportsman 570 ATVs because fuel can leak into the headlight pod, posing fire hazards.
Wildway LLC is recalling specific lots of Trader Joe's Grainless Granola due to potential contamination with Listeria monocytogenes.
Wildway LLC is recalling 442 cases of Vanilla Bean Espresso Grain-free Granola due to potential Listeria monocytogenes contamination.
AstraZeneca is recalling 40,368 bottles of BRILINTA 90 mg tablets because some bottles contained foreign Zurampic tablets.
SCA Pharmaceuticals is recalling 660 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The product was distributed in LA, PA, NY, and WI.
Baxter Healthcare is recalling 0.9% Sodium Chloride Injection bags due to customer complaints about leaking bags, which raises concerns about the product's sterility.
Sigan Industries is recalling CVS Health Baby Eczema Moisturizing Cream due to microbial contamination. The product failed to meet total plate count specifications.
Samiira's Homemade Muhammara Roasted Red Pepper Dip is being recalled because it may contain undeclared soy. Consumers should stop using the product.
Teva Pharmaceuticals is recalling 360 bottles of Paliperidone Extended-Release Tablets because one tablet failed a routine stability test for drug release.
Baxter Healthcare is recalling 54,528 bags of 5% Dextrose Injection because the bags may leak, compromising sterility.
Bristol-Myers Squibb is recalling 48,180 bottles of Eliquis 5mg tablets because one bottle was found to contain 2.5mg tablets instead.
Daimler Trucks is recalling specific 2017-2018 Freightliner and Western Star trucks because a fuel pump drive gear may slip, causing sudden engine stalls and increasing crash risk.
SCA Pharmaceuticals is recalling 20 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The affected product was distributed in LA, PA, NY, and WI.
SCA Pharmaceuticals is recalling 20 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The affected product was distributed in LA, PA, NY, and WI.