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. 2,580 recalls have been distributed to Nebraska in the last 12 months.
Showing 12881–12900 of 49,150 recalls
Recalled Item: Item # 744-4875 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 743-0278 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q Recalled by...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin 2 PCS MER3700 programmer Model MER3400 software Recalled by St. Jude...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant VR Implantable Cardioverter Defibrillator REF # CDVRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Microbiology Informatics Solution Recalled by Becton Dickinson &...
The Issue: When updating BD Kiestra customers to BD Synapsys version 4.10, the custom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RocheDiabetes Care Platform Software version 2.5.2 material number...
The Issue: Potential for patient data mismatch when using browser "back" button to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0mm x 10mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...
The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0mm x 12mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...
The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Standard PVC Laryngeal Masks Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The mask cuff may disconnect from the device's breathing tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sermorelin Acetate Lyophilized powder for reconstitution Recalled by Olympia...
The Issue: Sub Potent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxocobalamin B12 1mg/mL Recalled by Olympia Compounding Pharmacy dba...
The Issue: Sub Potent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sincalide Lyophilized powder for reconstitution Each ML contains: Mannitol...
The Issue: Super Potent and Failed Reconstitution Time
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: T-105 Recalled by Olympia Compounding Pharmacy dba Olympia Pharmacy Due to...
The Issue: Super Potent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula F9 Recalled by Olympia Compounding Pharmacy dba Olympia Pharmacy Due...
The Issue: Sub Potent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SB-4 Recalled by Olympia Compounding Pharmacy dba Olympia Pharmacy Due to...
The Issue: Sub Potent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NAD+ Nicotinamide Adenine Dinucleotide Recalled by Olympia Compounding...
The Issue: Product found to be Sub Potent or Exceeded reconstitution time
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Schwan's Spinach & Artichoke Dip. Item Number 061353 Recalled by Fairmont...
The Issue: Cartons of Spinach Artichoke Dip may contain Chicken & Broccoli.
Recommended Action: Do not consume. Return to store for a refund or discard.