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 Heparin Sodium 30,000U/30ML Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling 45 containers of Sermorelin Injection because the product lacks assurance of sterility. The recall covers distribution in eight US states.
Western Drug is recalling Testost CYP 200mg/mL SUS due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Western Drug is recalling M-Cobalamin (B12) injections because the FDA determined there is a lack of assurance of sterility. The recall affects 3 containers distributed nationwide.
Western Drug is recalling Prostin Injection due to a lack of assurance of sterility. The recall covers 16 containers distributed nationwide.
Western Drug Inc. is recalling 17 containers of Medroxyprogesterone 150/LID 5 mg/mL Injection because the company cannot ensure the product is sterile.
Custom Foods Inc. is recalling Founders Pride Chocolate Chip Cookies because they may be contaminated with peanuts. The product was distributed to restaurants in seven states.
Western Drug is recalling Calcium Chloride Dihydrate Injection because there is a lack of assurance of sterility. The product was distributed nationwide in eight states.
Western Drug is recalling Lidocaine Injection 1% and 2% due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Life Science Pharmacy Inc. is recalling BI-EST Creams because they may be contaminated with penicillin. The recall covers all lots distributed nationwide.
Western Drug Inc. is recalling 39 containers of Testosterone Injection due to a lack of assurance of sterility. The products were distributed nationwide in eight states.
Western Drug is recalling Wilson's Nasal Irrigation Solution because the product lacks assurance of sterility. The recall affects two containers distributed nationwide.
Western Drug is recalling four containers of Dexpanthanol B5 250mg/mL Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.
Western Drug is recalling Calcium Gluconate 10% Injection because the product lacks assurance of sterility. The recall covers two containers distributed nationwide.
Western Drug is recalling four containers of Super B Complex w/Cyano Inj due to a lack of assurance of sterility. The product was distributed nationwide in eight states.
Western Drug is recalling Alcohol 4%/Bupivicaine 0.5% solution because there is a lack of assurance of sterility. The product was distributed nationwide in eight states.
Philips Medical Systems is recalling three INTEGRIS vascular systems because the monitor ceiling suspension system may fall.
Western Drug Inc. is recalling 5 containers of Marcaine 0.24%/Ethanol 4% Injection because the product lacks assurance of sterility.
Life Science Pharmacy Inc. is recalling TRI-EST Lozenges due to potential penicillin cross-contamination. The recall covers all lots distributed nationwide.
Western Drug Inc. is recalling four containers of VitB12/VitC/VitB3/VitB9 Inj due to a lack of assurance of sterility.
Western Drug is recalling 46 containers of Methylcobalamin Injection because there is a lack of assurance of sterility.
Halcore Group is recalling 18 model year 2015 Horton ambulances because an incorrectly installed circuit board component may cause electrical system failure, potentially disabling life-saving equipment.
Life Science Pharmacy Inc. is recalling compounded Estriol Suppositories because they may be contaminated with penicillin. The recall covers all lots distributed nationwide.
Baylis Medical Corp is recalling 433 ProTrack Microcatheters nationwide due to circumferential cracks along the shaft.
Carl Zeiss Meditec is recalling IOL Master 500 software versions 7.5 and 7.7 because calculation printouts and exported reports may contain incorrect intraocular lens power data.