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. 1,129 recalls have been distributed to Indiana in the last 12 months.
Showing 6881–6900 of 29,228 recalls
Recalled Item: Medtronic XPANSE Bone Insert: a) DBM T600106 XPANSE SMALL-C 6 Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Gel: a) DBM S41120 GRAFTON GEL 1CC Recalled by Medtronic...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Orthoblend: a) DBM S44125 5CC ORTHOBLEND LARGE DEFECT...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System PA Sensor and Delivery System Recalled by St. Jude...
The Issue: Select CardioMEMS PA Sensors (Model CM2000) operate outside of the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Hoffmann LRF Recalled by Stryker GmbH Due to Stryker has identified...
The Issue: Stryker has identified a nonconformance in specific lots of Hoffmann LRF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to a failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Patient Electronics System (PES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Model Nos. 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85...
The Issue: An unexpected shutdown of the IABP may occur due to loss of communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to a failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: There have been reported failures of the high pressure helium regulator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Patient Electronics System (PES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Patient Electronics System (PES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Hospital Electronics System (HES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System PA Sensor and Delivery System Recalled by St. Jude...
The Issue: Select CardioMEMS PA Sensors (Model CM2000) operate outside of the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Model Nos. 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33...
The Issue: An unexpected shutdown of the IABP may occur due to loss of communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue. Model Number: 0998-00-0800-83. Recalled by Datascope...
The Issue: Firm has received reports of damaged, worn, or torn O-rings on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump. Model Numbers: D998-00-0800-31...
The Issue: Firm has received reports of damaged, worn, or torn O-rings on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System PA Sensor and Delivery System Recalled by St. Jude...
The Issue: Select CardioMEMS PA Sensors (Model CM2000) operate outside of the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: There have been reported failures of the high pressure helium regulator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA comprises AST Filters in conjunction with VITEK MS Recalled by...
The Issue: For users with MYLA V4.8.X / V4.9 that use VITEK MS to identify organisms as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.