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.
Hyundai is recalling 2018 Genesis G80 and G90 vehicles because incorrect primer may reduce windshield and rear window bonding strength, increasing crash risk.
General Motors is recalling 2016-2018 Chevrolet Cruze LS vehicles because they may leak gasoline after a rear-impact crash and rollover, increasing fire risk.
Target is recalling 2,652 pints of Ben & Jerry's Glampfire Trail Mix in Hawaii because a shipping container was not held at the proper temperature, potentially allowing contamination.
AuroMedics Pharma LLC is recalling Linezolid Injection bags due to a lack of assurance of sterility and a confirmed report of leaking bags with mold.
Target is recalling Halo Top Caramel Macchiato ice cream sold in Honolulu due to improper temperature control during shipping, which may have allowed contamination.
Target is recalling 2,652 units of Breyers 48oz Oreo Chips Ahoy 2 in 1 ice cream sold in Honolulu, HI, due to improper temperature control during shipping.
Target is recalling 2,652 units of Gardein Crispy Chick N Sliders sold in Hawaii because a shipping container was not held at the proper temperature, potentially allowing contamination.
Giovanni Food Company is recalling Parade Salsa Medium due to potential glass contamination. Consumers should stop using the product.
AuroMedics Pharma LLC is recalling 261,250 bags of Levetiracetam Injection due to a confirmed report of leaking bags and mold found between the outer bag and overwrap.
Target is recalling Enlightened Cookies & Cream ice cream pints sold in Hawaii because a shipping container was not held at the proper temperature, posing a potential contamination risk.
Target is recalling Halo Top S'mores ice cream sold in Hawaii because a shipping container was not held at the proper temperature, potentially allowing contamination.
AuroMedics Pharma LLC is recalling 308,112 bags of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and a confirmed report of mold.
Independent Nutrition, Inc. is recalling Ignite High Endurance Pre-Workout Supplement Vanilla because the label declared whey protein but failed to declare milk.
Target is recalling Breyers Delights Raspberry Chocolate ice cream in Hawaii because a shipping container was not held at the proper temperature, potentially allowing contamination.
Riddhi USA Inc. is recalling all dietary supplements it manufactures and distributes in New York, Delaware, and New Jersey pursuant to a Consent Decree.
Philips is recalling 184 MultiDim Eleva imaging systems because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
Philips is recalling 37 MultiDiagnost Eleva imaging systems because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
Target is recalling Popsicle Fruit Pop Mango units sold in Hawaii because a shipping container was not held at the proper temperature, potentially allowing contamination.
AuroMedics Pharma LLC is recalling Levetiracetam Injection due to a lack of assurance of sterility and a confirmed report of leaking bags and mold.
PerkinElmer is recalling Specimen Gate Screening Center software due to potential errors in neonatal screening results, including false negatives and positives.
Philips is recalling 199 MD-Eleva imaging systems because a tilt actuator may break, causing the table to rotate uncontrollably at high speed.
Target is recalling Enlightened Movie Night Pint products in Hawaii because a shipping container was not held at the proper temperature, potentially allowing contamination.
Philips is recalling 206 MD-Eleva imaging systems because the tilt actuator fixation may break, causing the table to rotate uncontrollably at high speed.
Zimmer Biomet is recalling 18 modular hip head components because two lots of different sizes were potentially commingled. This may lead to the use of an incorrect sized head.
Target is recalling 2,652 units of Old Orchard Apple Juice 100% 12oz in Hawaii because a shipping container was not held at the proper temperature, posing a risk of contamination.