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. 2,413 recalls have been distributed to Nebraska in the last 12 months.
Showing 35501–35520 of 49,150 recalls
Recalled Item: Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Single...
The Issue: The firm identified a malfunction which made it possible for a handpiece to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension RxL Max w/o HM Product Recalled by...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost stationary X-ray system Recalled by Philips...
The Issue: The detector may signal that it is ready for acquisition when it actually is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Bone Awl Recalled by Aesculap, Inc. Due to The flexible shaft of...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PerCoBa Whey Protein Isolate with Colostrum Recalled by Immuno - Dynamics,...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: French Style Green Beans packaged under the following labels: 1. Giant Eagle...
The Issue: The 16 oz poly bags of IQF French Style Green Beans have the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PerCoBa Colostrum Capsules Recalled by Immuno - Dynamics, Inc Due to The...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PerCoBa 1 Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand and...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Colostrum Lozenges Recalled by Immuno - Dynamics, Inc Due to The PerCoBa...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Colostrum Powder Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand...
The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips Healthcare DigitalDiagnost stationary X-ray system Recalled by...
The Issue: The detector may signal that it is ready for acquisition when it actually is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prednisone 20 mg Recalled by Northwind Pharmaceuticals LLC Due to Labeling:...
The Issue: Labeling: Not elsewhere classified. NDC number is incorrect on the container.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baclofen USP powder Recalled by Freedom Pharmaceuticals Inc Due to Presence...
The Issue: Presence of Foreign Substance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Spice Sage Ground Flax Seed Meal under the following Recalled by Zenobia...
The Issue: Zenobia Company, LLC is recalling Flax Seed Meal due to the possible...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic InSync III Recalled by Medtronic Inc. Due to Medtronic has...
The Issue: Medtronic has confirmed an issue with InSync III CRT-pacemaker devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun Temperature Management System Recalled by C.R. Bard, Inc. Due to...
The Issue: The product may contain electronic components that lead to a premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remote Patient Monitoring System Recalled by Vidco, Inc. Due to Testing at...
The Issue: Testing at customer site showed unit Remote Patient Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10) Recalled...
The Issue: Antibiotic concentration may be insufficient which may result in incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unolok Blunt Fill Needle 18G x 1.5" Red Recalled by Myco Medical Supplies...
The Issue: Particulates: Complaints of rubber coring from the closure of injection vials.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Destination Renal Guiding Sheath Intended for the introduction of...
The Issue: Based on internal investigation and testing that revealed the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.