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. 1,132 recalls have been distributed to Nebraska in the last 12 months.
Showing 1421–1440 of 49,150 recalls
Recalled Item: Everolimus tablets 5mg Recalled by Endo USA, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclophosphamide Injection 500 mg/5 mL (100 mg/mL) Recalled by Sandoz Inc...
The Issue: cGMP deviations: Temperature excursion during transportation.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...
The Issue: Due to display cables used for monitors were not in compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Apotex Corp. Due to...
The Issue: Lack of Assurance of Sterility; atypical weight loss due to improper bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution Recalled by Apotex...
The Issue: Lack of Assurance of Sterility; atypical weight loss due to improper bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AW Server 2.0 Recalled by GE Medical Systems, SCS Due to Firm has identified...
The Issue: Firm has identified a security vulnerability in AW Server products. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description BFCT04X CATARACT PACK -...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halved Pears IN PEAR JUICE FROM CONCNETRATE Recalled by Pacific Coast...
The Issue: Potential contamination with heavy metal (Lead).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Good and Gather brand Southwest-Style Burrito Bowl Blend Processed in...
The Issue: Product may contain undeclared shrimp (crustacean shellfish).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pears SLICED in Organic Pear Juice from Concentrate Recalled by Pacific...
The Issue: Potential contamination with heavy metal (Lead).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pears Halves in Pear Juice from Concentrate Recalled by Pacific Coast...
The Issue: Potential contamination with heavy metal (Lead).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fruit Cocktail IN 100% JUICE WITH ADDED INGREDIENTS Recalled by Pacific...
The Issue: Potential contamination with heavy metal (Lead).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Basic Biopsy Tray Recalled by American Contract Systems Inc. Due to...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits IHDC30R D AND C PACK Recalled by American Contract...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description ANSH14AF SHOULDER PACK -...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description ANCV78BC HEART PACK -...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description EVLH67F LEFT HEART CATH...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XERF EFFECTOR 60. Electrosurgical unit. Recalled by Lutronic Corporation Due...
The Issue: Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL LINE...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.