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. 2,547 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,547 in last 12 months

Showing 2852128540 of 53,528 recalls

Medical DeviceDecember 8, 2017· Datex-Ohmeda, Inc.

Recalled Item: CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The...

The Issue: Potential for the display processor to experience an unexpected failure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Remel Inc

Recalled Item: Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum Recalled by Remel Inc...

The Issue: The serum may fail to agglutinate within the specified minimum reaction time.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c8000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely depressed patient results in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Humeral Stem 55mm(Size 13) Product Usage: Intended for primary and Recalled...

The Issue: Zimmer Biomet is conducting a medical device recall for two lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2017· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely depressed patient results in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: PROPONENT MRI Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO MRI DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ALTRUA 2 DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: PROPONENT VDD SL Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: VISIONIST X4 CRT-P Pacemaker Recalled by Boston Scientific Corporation Due...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: VALITUDE X4 CRT-P Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO MRI EL DR Pacemaker Recalled by Boston Scientific Corporation Due...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO MRI SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ALTRUA 2 SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE MRI SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing