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. 1,069 recalls have been distributed to Nebraska in the last 12 months.
Showing 14261–14280 of 49,150 recalls
Recalled Item: ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg Recalled by...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Advance Formula Pain Reliever (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Loratadine-D Extended-Release Tablets (Loratadine and Pseudoephedrine...
The Issue: Failed Moisture Limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methocarbamol 500mg Tablet Recalled by Bryant Ranch Prepack, Inc. dba BRP...
The Issue: Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: CGMP Deviations: Lots recalled because they were manufactured at the same...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: CGMP Deviations: Lots recalled because they were manufactured at the same...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AllerClear D-24 hr Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Failed Moisture Limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artis icono biplane with software VE20C-diagnostic imaging angiography...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Device Manager application software (D00U005)...
The Issue: The processing of collected episode data may fail due to a software error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono floor with software VE20C-diagnostic imaging angiography system...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno with software VE20C- diagnostic imaging angiography system...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion kits Recalled by Medtronic Perfusion Systems Due...
The Issue: Product is labeled as non-pyrogenic but endotoxin testing was not performed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant 3.5x10 Recalled by Jjgc Industria E Comercio De...
The Issue: 3.5x11.5mm implants were mislabeled as 3.5x10mm implants. In borderline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.