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.
Creation's Garden Natural Products is recalling Welltrients Digestaids Formula #2 capsules because they contain chloramphenicol.
CGNP Manufacturing is recalling Beach Body Ultimate Reset Kit 2.0 because the raw material used in the formulation contains chloramphenicol.
Empirical Labs is recalling specific lots of Building Health Thyroid dietary supplements due to potential adulteration with chloramphenicol.
Empirical Labs is recalling Natural Balanced Nutrition Vanilla Energy Shake dietary supplements due to potential adulteration with chloramphenicol.
CGNP is recalling Beachbody Optimize Enzymes Capsules because the raw material used contains chloramphenicol. The recall covers 500 bottles distributed in California.
Priester Pecan Company is recalling specific lots of roasted salted pistachios due to potential Salmonella contamination. The product was distributed nationwide and in Puerto Rico.
Quaker Foods and Snacks North America is recalling Aunt Jemima Quick Grits because some bags contain aflatoxin levels above the legal limit.
ProThera, Inc. is recalling Klaire Labs Vital-Zymes complete enzyme supplements because the enzymes may be contaminated with chloramphenicol.
Quaker Foods and Snacks North America is recalling specific lots of Aunt Jemima Quick Grits and Corn Meal Mix because they contain aflatoxin above legal limits.
Empirical Labs is recalling specific lots of P&L Enzymes dietary supplements due to potential adulteration with chloramphenicol.
Viking is recalling about 750 built-in side-by-side refrigerator freezers because electrical connectors can overheat, posing a fire hazard. Consumers should unplug the units and contact Viking for a free repair.
Suzuki is recalling 2013 SX4 vehicles with continuously variable transmissions because torque converter bolts may loosen, potentially causing the engine to stall and increasing crash risk.
PACCAR is recalling 2007-2014 Kenworth T800 and W900 trucks because brake chambers may take too long to apply or release, increasing crash risk.
BMW is recalling 2013 X3 xDrive 28i/35i vehicles because a production error in the instrument panel could cause the airbag to deploy improperly during a crash.
Bridgestone is recalling Firestone HP3000 tires sold in Guam because a crack in the inner liner may cause a sidewall bulge and tire failure.
Honda is recalling 2014 Acura MDX AWD vehicles because drive shaft bolts may not be properly tightened, which could allow the shaft to detach and increase crash risk.
Yoders Country Market is recalling 24 units of Honey Roasted Peanuts in custom gift boxes because the product contains undeclared milk and wheat.
Safeway is recalling 70,162 units of Angel Food Cake because the labels omitted milk and soy ingredients, posing a risk to consumers with allergies.
Hospira Inc. is recalling 70,450 vials of Propofol Injectable Emulsion because visible particles were found in the glass during inspection.
Mylan Pharmaceuticals is recalling specific lots of Amlodipine Besylate and Benazepril HCl capsules because they were not manufactured according to Good Manufacturing Practices.
J M Smucker is recalling White Lily Corn Meal Self-Rising because aflatoxin levels exceeded FDA specifications in independent testing.
J M Smucker is recalling specific lots of Martha White and White Lily cornmeal because aflatoxin levels exceeded FDA specifications.
Baylis Medical is recalling TorFlex Transseptal Guiding Sheath Kits because the sheath may remove particulate from the dilator, which could migrate into a patient's bloodstream.
American Laboratories Inc is recalling specific lots of EB 110311-01 enzyme blend powder because the products may be contaminated with Chloramphenicol.
Irwin Naturals is recalling Dual Action Cleanse and Daily Digestive Enzymes because they may be contaminated with chloramphenicol.