Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,747 recalls have been distributed to Indiana in the last 12 months.
Showing 4901–4920 of 29,228 recalls
Recalled Item: BD BBL Sensi Disc Augmentin - 3¿g 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 Sulfamethoxazole with Trimethoprim 23.75/1.25 ug Recalled...
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 Ceftazidime- 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 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.
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: 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 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: 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 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: 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 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 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 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: OPTIMIZER model CCM X11 implantable pulse generator (IPG) devices - Recalled...
The Issue: OPTIMIZER devices may cease to deliver CCM therapy if the device incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Contro-Bulb Syringe Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Packaging material was updated for the Bulb Irrigation Syringe (DYND20125),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...
The Issue: A software error caused an increase in tray gripper motion errors that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USTAR II Knee System Cemented curved stem Recalled by United Orthopedic...
The Issue: Their is a potential that the implant curved stem may be oriented incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USTAR II Knee System : Cemented Curved Stem Recalled by United Orthopedic...
The Issue: Their is a potential that the implant curved stem may be oriented incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USTAR II Hip System Press-Fit Curved Stem Recalled by United Orthopedic...
The Issue: Their is a potential that the implant curved stem may be oriented incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse Cardiology PACS V7.3.0 Recalled by FUJIFILM Healthcare Americas...
The Issue: The LV Mass (2D Bullet) equation may be calculated incorrectly, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.