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. 2,617 recalls have been distributed to Nebraska in the last 12 months.
Showing 6901–6920 of 49,150 recalls
Recalled Item: MB362R - JACOBSON DUROGRIP TC Micro Needle Holder Recalled by Aesculap Inc...
The Issue: Needle Holder MB215R was inadvertently distributed as MB362R. Similarly,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips North America Due to An incorrect electrical...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Due to An...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Due to An...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag Recalled...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FentaNYL citrate PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VANCOmycin HCl PF 1.5g added to 0.9% Sodium Chloride 250 mL IV bag Recalled...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FentaNYL citrate PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 20 mg per 250 mL 0.9% Sodium Chloride (80 mcg per mL)...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 40 mg per 250 mL 0.9% Sodium Chloride (160 mcg per mL)...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DELFLEX Peritoneal Dialysis Solution in Biofine container 1.5% Dextrose...
The Issue: Lack of Sterility Assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe Recalled by MRP,...
The Issue: The saline flush syringes may fail to meet USP criteria for stated sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung Digital Diagnostic Mobile X-ray System Recalled by NeuroLogica...
The Issue: Mobile x-ray systems moving arm frame welding issue which presents the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.