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. 1,095 recalls have been distributed to Nebraska in the last 12 months.
Showing 6821–6840 of 49,150 recalls
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custodiol HTK Solution Recalled by Dr Franz Koehler Chemie Gmbh Due to...
The Issue: Potential for particles to be present in solution.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...
The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Budesonide Extended-Release Tablets 9mg Recalled by Teva Pharmaceuticals...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BEQ-RF-32-USA RotaFlow Centrifugal Pump with BIOLINE Coating Recalled by...
The Issue: Nonconformities at their seal could potentially compromise the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Clarithromycin- 15 ug Recalled by Becton Dickinson & Co....
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Ampicillin with Sulbactam 10/10 ¿g Recalled by Becton...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Doripenem- 15 ug Recalled by Becton Dickinson & Co. Due to...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Ceftriaxone- 30 ug Recalled by Becton Dickinson & Co. Due...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Cefuroxime- 30 ug Recalled by Becton Dickinson & Co. Due...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Ampicillin - 10 ¿g Recalled by Becton Dickinson & Co. Due...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BO-RF-32-USA RotaFlow Centrifugal Pump with SOFTLINE Coating Recalled by...
The Issue: Nonconformities at their seal could potentially compromise the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Cefixime - 5 ug¿ Recalled by Becton Dickinson & Co. Due to...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Sensi Disc Ofloxacin- 5 ug Recalled by Becton Dickinson & Co. Due to...
The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.