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. 2,725 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,725 in last 12 months

Showing 1018110200 of 29,228 recalls

Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Ilestro 7 DR-T Recalled by BIOTRONIK Inc Due to There is a...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK IPERIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Ilestro 7 VR-T Recalled by BIOTRONIK Inc Due to There is a...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Ilestro 7 DR-T Recalled by BIOTRONIK Inc Due to There is a...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Iforia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INTICA NEO 7 HF-T DF-1 IS-1 ProMRI Recalled by BIOTRONIK Inc Due...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Iforia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Iperia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA NEO 7 VR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INTICA NEO 7 VR-T DX DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing