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. 2,059 recalls have been distributed to Indiana in the last 12 months.
Showing 6241–6260 of 29,228 recalls
Recalled Item: SurgiMend Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend MP Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revize-X Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend PRS Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Ag Meshed Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TissueMend Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend 2.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Meshed Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend 4.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revize Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend PRS Meshed Recalled by TEI Biosciences, Inc. Due to Possible out...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis CII Safe Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated dispensing cabinet devices plugged into any multi-socket outlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-10 Recalled by...
The Issue: There are potential risks of the Hemospray powder adhering to the distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-7 Recalled by...
The Issue: There are potential risks of the Hemospray powder adhering to the distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour¿ next GEN Blood Glucose Monitoring System Recalled by Ascensia...
The Issue: Ascensia Diabetes Care has determined through customer complaints that 580...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroPass Ureteral Access Sheaths Recalled by Olympus Corporation of the...
The Issue: Dilator tips may break in the package and in patients during surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voalte Patient Safety Recalled by Baxter Healthcare Corporation Due to...
The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Recalled by Philips North America Llc Due to There is a...
The Issue: There is a software login in issue that may prevent the user from logging in.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviCare Patient Safety V3.9.200 to 3.9.600 Recalled by Baxter Healthcare...
The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW Endurance Extended Dwell Peripheral Catheter System Recalled by ARROW...
The Issue: Potential for catheter separation or leakage
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.