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. 1,171 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,171 in last 12 months

Showing 1501–1520 of 53,528 recalls

Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 3, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Viorele Recalled by Glenmark Pharmaceuticals Inc., USA Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10C Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Chlorpromazine Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Kit for the Preparation of Technetium Tc 99m Mertiatide Recalled by SUN...

The Issue: Failed Dissolution Specifications-Out of Specification (OOS) observation for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Cardio Vascular-Allura Centron Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/15 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The BIOS battery may deplete faster than initially anticipated during the...

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

Class II — Potential Health HazardOngoing