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.
Alfred Louie Inc. is recalling 10-pound packages of mung bean sprouts because FDA environmental samples found Listeria monocytogenes in the facility.
Aston Martin is recalling specific 2012-2014 models because a manufacturing error may cause the throttle pedal arm to break, preventing the driver from maintaining or increasing engine speed.
Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Ball - Shrimp Ball because the label failed to list egg and the fish species.
Go Max Go Foods is recalling Thumbs Up Candy Bars labeled as dairy-free because they contain undeclared milk.
Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Balls because the label failed to list egg and the specific fish species.
Lloyd Inc. of Iowa is recalling 5.7 million Thyro-Tab tablets because stability failures in previous lots make it impossible to verify the quality of the current lots.
Win Luck Trading Inc. is recalling Lam Sheng Kee Frozen White Fish Balls because the label failed to list egg as an ingredient and did not declare the species of fish.
Triumph is recalling 2012-2013 Trophy and Trophy SE motorcycles because the fuel tank layers may fail to adhere, causing leaks that could lead to engine stalls or fires.
Yakima is recalling Whispbar rack fitting kits for specific vehicles because they do not fit the roofline properly, creating a crash risk.
Green Valley Drugs is recalling 529 vials of Magnesium Sulfate Injection because the pharmacy could not ensure the products were sterile.
Insolroll is recalling about 1,500 solar and rechargeable motor roller shades because the built-in lithium batteries can overheat and cause fires.
Green Valley Drugs is recalling Lipotropic With Vitamins, Carnitine, Chromium and Glutamine Injection because the pharmacy could not ensure the products were sterile.
Green Valley Drugs is recalling Modified Myers Cocktail Injection vials because the pharmacy could not ensure the products were sterile.
Green Valley Drugs is recalling Estradiol Cypionate Injection because the pharmacy could not ensure the products were sterile. The recall covers all strengths and presentations distributed nationwide.
Lisy Corp. is recalling Adobo sin pimienta in 5 oz, 14 oz, and 32 oz sizes because the product contains undeclared soy.
Green Valley Drugs is recalling L-Lysine Injection vials because the pharmacy could not ensure the products were sterile.
Performance Plus Marketing, Inc. is recalling Libigrow capsules marketed without FDA approval. The product may contain undeclared sildenafil, tadalafil, and analogues.
Green Valley Drugs is recalling 1,140 vials of Gentamicin Injection nationwide due to a lack of assurance of sterility in its compounding and quality control processes.
Green Valley Drugs is recalling L-Carnitine Injection nationwide due to a lack of assurance of sterility in its compounding and quality control processes.
Green Valley Drugs is recalling Betamethasone Sodium Phosphate Injection because the pharmacy could not ensure the sterility of the compounded products.
Green Valley Drugs is recalling Hydrochloric Acid Injection products because of a lack of assurance of sterility and quality control concerns.
Green Valley Drugs is recalling Testosterone Cypionate Injection vials and syringes because the compounding pharmacy could not ensure the products were sterile.
Green Valley Drugs is recalling Edetate Calcium Disodium Injection due to a lack of assurance of sterility in its quality control processes.
Lisy Corp. is recalling Sazon Fajita seasoning in 5 oz, 14 oz, and 28 oz sizes because it contains undeclared soy. The product was distributed in 12 states.
FVS Holdings, Inc. dba. Green Valley Drugs is recalling 65 vials of Metoprolol Injection due to lack of assurance of sterility and quality control concerns.