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.
Baptist Health Medical Towers Pharmacy is recalling 16 bags of Clindamycin 900 mg in 100 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 59 bags of Vancomycin 1000 mg in 250 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 7 bags of 1/2 Normal Saline due to lack of sterility assurance. The product was distributed in Arkansas.
Baptist Health Medical Towers Pharmacy is recalling five Deferoxamine cassettes in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 22 bags of Meropenem 2 grams in 100 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 11 bags of Vancomycin IV solution in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling six D5 1/2 NS IV fluid bags in Arkansas due to a lack of sterility assurance.
Forest River is recalling 2015 Glaval Synergy transit buses because steering boxes may wear prematurely, risking loss of steering control.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
Baptist Health Medical Towers Pharmacy is recalling 24 bags of Invanz 1 gram in 100 mL 0.45% NS due to lack of sterility assurance.
Liquid Assets Inc. is recalling Angel Wings and Magzuma dietary supplements because they contain undeclared milk and soy allergens.
Baptist Health Medical Towers Pharmacy is recalling 86 bags of TPN 2 in Arkansas due to a lack of sterility assurance.
FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.
Baptist Health Medical Towers Pharmacy is recalling Dobutamine IV bags in Arkansas due to a lack of sterility assurance.
Newmar is recalling 2014-2016 Dutch Star motorhomes because a defective steering box may cause loss of steering control.
Terex Advance is recalling 338 model year 2016 Front Discharge Concrete Mixer trucks because a weld failure could cause the main chute to detach while driving, increasing crash risk.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
Baptist Health Medical Towers Pharmacy is recalling 11 bags of Cefazolin 6 grams in 292 mL 0.9% NS due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 7 bags of Water for Injection in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy recalled Deferoxamine syringes in Arkansas due to lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling three bags of Hydromorphone 2 mg/mL IV solution in Arkansas due to a lack of sterility assurance.
Baptist Health Medical Towers Pharmacy is recalling 11 bags of Nafcillin 12 grams in 322 mL 0.9% NS due to a lack of sterility assurance.
Bridgewell Resources LLC is recalling Ivory Teff Flour due to potential Salmonella contamination. The product was distributed in California and Washington.
Pronutri, LLC is recalling 356 bottles of Re-VITA-lize Tropical Orange Dietary Supplement due to undeclared milk and soy lecithin.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility caused by a breach of the barrier.