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. 2,384 recalls have been distributed to Nebraska in the last 12 months.
Showing 41041–41060 of 49,150 recalls
Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...
The Issue: The temperature probe does not properly connect to the temperature port.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIRACEPT (R) (nelfinavir mesylate) Tablets Recalled by Pfizer Inc. Due to...
The Issue: Labeling: Incorrect or missing lot and or Exp Date: The bottles were labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shell Eggs packaged under the following labels: (1) Abbotsford Farms...
The Issue: Shell eggs contaminated with Pseudomonas fluorescens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Choripdong Chocolate Almond Richmond Ice Bar 4 bars/432 mL Seoul Recalled by...
The Issue: Seoul Trading USA Inc. is recalling Choripdong Chocolate Almond Richmond Ice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gyrus ACMI Falope-Ring Dilator Recalled by Gyrus Medical, Inc Due to...
The Issue: Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Luminos dRF Recalled by Siemens Medical Solutions USA, Inc Due to It...
The Issue: It was discovered that during a RAD examination using Siemens Luminos dRF,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Possible sound loss...
The Issue: Possible sound loss associated with the CARESCAPE Monitor B650. When an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4051 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4002S Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4052 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excella II Standard Pedicle Screw Recalled by Innovasis, Inc Due to Mislabeling
The Issue: Innovasis is recalling the Excella II Standard Pedicle Screw due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Succinate Extended-release Tablets Recalled by Mylan...
The Issue: Presence of Foreign Tablets/Capsules: A pharmacist reported a rogue tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....
The Issue: Failed PH Specifications: It has been determined that the pH of the lots...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.