Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,606 recalls have been distributed to Nebraska in the last 12 months.
Showing 10501–10520 of 13,356 recalls
Recalled Item: E2 (Estradiol (E2) Trit (Yellow) : E3 (Estriol USP Micronized Recalled by...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : Recalled by...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRIOL (E3) W/V (weight/volume) VERSABASE [4714] 0.05% (0.5MG/ML)...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 80/20 (estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3))...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 89/11 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3))...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRIOL 5 ESTRADIOL (Estradiol (E2) Trit (Yellow)) 0.95 ESTRONE (Estrone...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRIEST 80/10/10 (E1/E2 Trit - Estrone (E1)/Estradiol (E2) / Estriol Recalled...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 91/9 (Estriol USP Micronized (E3)/Estradiol (E2) Trit (Yellow))...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIEST TD 80/20 (Estradiol (E2) Trit (Yellow)/Estriol USP Micronized (E3)...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRIOL (E3) 2.5MG suppositories Recalled by the Compounder Due to Recalled...
The Issue: Recalled products were made using an active ingredient that was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Domperidone BP Recalled by Freedom Pharmaceuticals Inc Due to Penicillin...
The Issue: Penicillin Cross Contamination: Potential for products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA ZX DIETARY SUPPLEMENT (Extracto de Naranjo Amargo 70 Recalled by Ultra...
The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis confirmed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ergoloid Mesylates Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: during long-term stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fomepizole Injection Recalled by Navinta LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility. A recent FDA inspection reported GMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION Recalled by Hospira Inc. Due to...
The Issue: Labeling: Wrong Bar Code: There is a potential for some units to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% DEXTROSE Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: there is a potential for solution to leak at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Confirmed finding of human hair floating in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.