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.
Patel Grocery Corp is recalling America's Best Cumin Powder because it contains undeclared peanut protein, posing a risk to individuals with peanut allergies.
Waymouth Farms is recalling specific brands and sizes of raw pine nuts because they may be contaminated with Salmonella.
Texas Pecan Co. is recalling specific lots of Sweet-N-Salty Nuts because they may be contaminated with Salmonella.
Eldorado is recalling 2007-2015 Axess, XHF, and E-Z Rider II vehicles because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.
Keystone RV Company is recalling 2015 Keystone and Dutchmen fifth wheels because screws securing the expanding room may fail, increasing crash risk.
Superior Foods is recalling Simply Balanced Organic Chopped Spinach due to possible Listeria contamination. Consumers should not eat the product and should return it to the store.
Philips Medical Systems is recalling Pinnacle3 software version 10.0 because a defect in the dose engine may cause incorrect radiation therapy dose calculations.
GE Healthcare is recalling four CT scanners because over-torqued bolts could cause a component to detach, posing a risk of serious bodily injury.
Gouveia & Sons Imports is recalling Gouveia Crushed Red Pepper because it fails to declare FD&C Yellow #5 and sulfites.
Greystone Foods is recalling 11,004 bags of Today's Harvest Field Peas w/Snaps due to possible Listeria monocytogenes contamination. The product was distributed in Florida and Georgia.
Best Foods NJ, Inc. is recalling Deer Cumin Powder in 7 oz and 14 oz packages due to undeclared peanuts.
Crane Carrier is recalling 630 model year 2008-2015 COE, LDT2, and LET2 trucks because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.
PACCAR is recalling specific Kenworth and Peterbilt trucks because a driveshaft weld may fail due to corrosion, potentially causing loss of power to the rear wheels.
Chrysler is recalling 2003 Dodge Ram trucks because the passenger air bag inflator may rupture during deployment, potentially causing serious injury or death.
PACCAR is recalling specific Kenworth and Peterbilt trucks because a vent tube may detach, allowing engine oil to contact hot surfaces and cause a fire.
MACVAD is recalling Auto XS Heated Seat Covers manufactured between August and September 2014 because they may overheat and melt, posing injury or fire risks.
Viking Range is recalling approximately 52,000 gas ranges in the U.S. because the ovens can turn on by themselves, posing a burn hazard.
Fallon Wellness Pharmacy is recalling Methylcobalamin/Hydroxocobalamin injections due to a lack of assurance of sterility. The affected product was distributed in New York.
Whole Foods Market is recalling Black Bean Dip because it contains undeclared peanut protein. Consumers with peanut allergies should not eat the product.
Health Innovations Pharmacy is recalling Glycopyrrolate 0.2 mg/1 mL Suspension (Robinul) because inspection findings indicate a lack of assurance regarding sterility and stability data.
Health Innovations Pharmacy is recalling Dexamethasone 4 mg/mL Iontophoresis solution because inspection findings raised concerns about sterility and stability data.
Mission Pharmacal is recalling 2,412 kits of Sodium Sulfacetamide 9% and Sulfur 4.5% Wash due to microbial contamination.
Health Innovations Pharmacy is recalling Serum 50% BSS 50% Opth Drops due to lack of assurance of sterility and stability data. The recall covers all lots distributed in North Carolina.
Fallon Wellness Pharmacy is recalling Methylcobalamin/B-Complex Injection vials due to a lack of assurance of sterility. The affected product was distributed in New York.
Health Innovations Pharmacy is recalling Voriconazole 1% Opth Drops due to quality control issues affecting sterility and stability data.