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. 2,177 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,177 in last 12 months

Showing 40414060 of 53,528 recalls

DrugNovember 4, 2024· Boulla LLC

Recalled Item: PeakMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: ZoomMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2024· Tipp Distributors, Inc. dba Novamex

Recalled Item: Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton Recalled by Tipp...

The Issue: The hermetic seal on the lid of the cans may be compromised

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: VitalityXtra Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: ZapMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2024· The JM Smucker Company LLC

Recalled Item: Great Value Cheese Danish 16.5 oz Recalled by The JM Smucker Company LLC Due...

The Issue: Pieces of plastic in product

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2024· The JM Smucker Company LLC

Recalled Item: Great Value Cinnamon Rolls 16.5oz Recalled by The JM Smucker Company LLC Due...

The Issue: Pieces of plastic in product

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· JR Watkins

Recalled Item: Cooling Menthol Extra Strength Pain Relief Patch Recalled by JR Watkins Due...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 1, 2024· Medtronic Neurosurgery

Recalled Item: Becker External Drainage and Monitoring System: 24146 EDMS 24146 BECKER...

The Issue: Due to complaints received reporting cracks and/or leaks of the stopcocks...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 1, 2024· Securitas Healthcare LLC

Recalled Item: Arial Server Software Versions 11.1.4 through 11.1.6 Recalled by Securitas...

The Issue: Certain software versions will not notify end users of calls initiated by...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: FACSLyric 2L4C Instrument US Recalled by Becton, Dickinson and Company, BD...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: FACSLyric 3L12C Instrument RUO Recalled by Becton, Dickinson and Company, BD...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Becton, Dickinson and Company, BD Bio Sciences

Recalled Item: FACSLyric 3L10C Instrument US-IVD Recalled by Becton, Dickinson and Company,...

The Issue: On October 18, 2024, BD has identified through customer complaints and an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2024· Cardinal Health 200, LLC

Recalled Item: Cardinal Health SMS Elastic Cuff Thumbhook Level 3 Isolation Gown Recalled...

The Issue: Isolation Gowns were manufactured with raw materials that may fail the...

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

Class II — Potential Health HazardOngoing