State
73,827 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.
Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.
Which agencies issued them
These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Western Drug is recalling Sodium Hydroxide 10% Injection because the company cannot ensure the product is sterile. The recall covers all lots distributed nationwide.
Philips Medical Systems is recalling 22 Allura Xper vascular systems because the monitor ceiling suspension system may fall.
Western Drug is recalling six containers of Tev-Tropin (Somatropin) Injection due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Life Science Pharmacy Inc. is recalling compounded Estriol Creams nationwide because they may be contaminated with penicillin.
Life Science Pharmacy Inc. is recalling Hydroxocobalamin Injection due to potential penicillin cross-contamination. The recall covers all lot numbers and expiration dates distributed nationwide.
Life Science Pharmacy Inc. is recalling Human Chorionic Gonadotropin (HCG) injections nationwide due to potential penicillin cross-contamination.
Western Drug is recalling Podophyllum 40% Topical because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Novarel HCG 10000U/Vial prescription vials nationwide due to a lack of assurance of sterility.
Newmar is recalling specific model year 1997-2005 motorhomes because a steering gear mounting bracket may crack, potentially causing a loss of steering ability.
Life Science Pharmacy Inc. is recalling compounded Estriol Face Creams because they may be contaminated with penicillin.
Western Drug is recalling Heparin 1000 Unit/mL Injection because the product lacks assurance of sterility. The recall covers two containers distributed nationwide.
Western Drug is recalling Magnesium Chloride Injection because the product lacks assurance of sterility. The recall covers two containers distributed nationwide.
Western Drug is recalling Depo-Testadiol 10/5mg/mL Injection because the product lacks assurance of sterility. The recall affects four containers distributed nationwide.
Western Drug Inc. is recalling four containers of Cyclosporine 1% Opth Sol because the product lacks assurance of sterility. The recall covers distribution in eight US states.
Western Drug is recalling Salicylic Acid Injections because the company cannot ensure the product is sterile. The recall covers all lots distributed nationwide.
Western Drug is recalling Calcium EDTA 300mg/mL Injection because the product lacks assurance of sterility. The recall affects two containers distributed nationwide.
Western Drug is recalling two containers of Potassium Chloride 40 mEq/mL Injection because the product lacks assurance of sterility.
Western Drug is recalling 15 containers of Quad Mix Inj because the company cannot ensure the product is sterile.
Western Drug is recalling Benadryl 50mg/2mL Pres-Free Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Super B Complex 3X Injections because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Life Science Pharmacy Inc. is recalling BI-EST Suspensions because they may be contaminated with penicillin. The recall covers all lots distributed nationwide.
Western Drug is recalling two containers of Tacrolimus 0.02% Opth Sol due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Western Drug is recalling Lipodissolve 100/50mg Injection Solution because the company cannot assure the product is sterile.
Western Drug is recalling Testosterone CYP Inj 200 mg/mL nationwide due to a lack of assurance of sterility.
Western Drug is recalling Bladder Mixture Prep because the product lacks assurance of sterility. The recall affects four containers distributed nationwide.