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. 1,077 recalls have been distributed to Indiana in the last 12 months.
Showing 16741–16760 of 53,528 recalls
Recalled Item: Spectrum IQ - Infusion Pump - Product Usage: intended to Recalled by Baxter...
The Issue: Potentially defective component in the AC power adapter which may fail over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protek Solo Venous Dilator Set: dilator Recalled by Cardiac Assist, Inc Due...
The Issue: On 02/26/2021, it was found that there were incorrectly packaged Dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer - Product Usage: intended to assist in the...
The Issue: When the Cross Enterprise Display option is enabled on the Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% Recalled...
The Issue: Microbial Contamination of Non-Sterile Product:.Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v...
The Issue: Microbial Contamination of Non-Sterile Product.Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v...
The Issue: CGMP Deviations: Product is being recalled because at labeled storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Product is being recalled because at labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD ChloraPrep Hi-Lite Orange 2% w/v chlorhexidine gluconate (CHG) and...
The Issue: Lack of Assurance of Sterility: Product is being recalled because at labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD ChloraPrep Hi-Lite Orange 2% w/v chlorhexidine gluconate (CHG) and...
The Issue: Non-sterility.Product is being recalled because at labeled storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% Recalled...
The Issue: CGMP Deviations: Product is being recalled because at labeled storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to...
The Issue: Non-sterility.Product is being recalled because at labeled storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neomycin Sulfate Tablets Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Failed Stability Specifications: Out of Specification (OOS) result reported...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaBplus and AquaBplus B2 Water Purification System - Product Usage:...
The Issue: AquaBplus HF module on the AquaBplus 2500 osmosis system, an error in the US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Processor SP - Product Usage: intended for processing and Recalled...
The Issue: Potential for a false-negative result for Vibrio parahaemolyticus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dental pins - TMS LINK PLUS Self-Threading Pins - Product Recalled by...
The Issue: The incorrect dental pins were packaged and subsequently distributed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentueri Viral Transport Medium (VTM) Recalled by Gentueri Inc Due to Medium...
The Issue: Medium showed visual turbidity and discoloration, potentially contaminating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment Recalled by...
The Issue: The firm discovered through customer complaints that device segments may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.