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. 1,929 recalls have been distributed to Indiana in the last 12 months.
Showing 24081–24100 of 29,228 recalls
Recalled Item: MOSAIQ Product Usage: MOSAIQ is an oncology information system used Recalled...
The Issue: A problem can exist in MOSAIQ resulting in the display of incorrect numeric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM PERMANENT CAUTERY SPATULA Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM FENESTRATED BIPOLAR FORCEPS Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM RESANO FORCEPS Recalled by Intuitive Surgical, Inc. Due to Deviations in...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM MONOPOLAR CURVED SCISSORS Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Deviations in reprocessing steps from those stated in the reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery System with the first generation IRIS...
The Issue: Software upgrade to correct potential safety issue related to CyberKnife...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITI VISION SYSTEM ULTRASOUND FMS. Single-use fluid management system....
The Issue: Alcon is conducting a medical device recall due to the possible presence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crea A and B membranes Recalled by Radiometer America Inc Due to Negative...
The Issue: Negative drift on QC during in-use lifetime of CREA membranes can be observed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.