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. 2,696 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,696 in last 12 months

Showing 1336113380 of 53,528 recalls

DrugMarch 10, 2022· Macleods Pharma Usa Inc

Recalled Item: Risedronate Sodium Tablets Recalled by Macleods Pharma Usa Inc Due to FAILED...

The Issue: FAILED CONTENT UNIFORMITY SPECIFICATIONS

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

Class III — Low RiskOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 721-1000 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 744-4930 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 714-5000 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 721-0200 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 722-0105 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 714-0706 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 731-0120 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 744-4875 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 743-0278 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q Recalled by...

The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q Recalled...

The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin 2 PCS MER3700 programmer Model MER3400 software Recalled by St. Jude...

The Issue: Due to a programmer software anomaly under very specific circumstance when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...

The Issue: Due to a programmer software anomaly under very specific circumstance when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Gallant VR Implantable Cardioverter Defibrillator REF # CDVRA500Q Recalled...

The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...

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

Class II — Potential Health HazardOngoing
FoodMarch 9, 2022· Taylor Farms

Recalled Item: Taylor Farms - Thai Noodle Salad Kit packaged in 108oz Recalled by Taylor...

The Issue: Downstream Recall - Foreign Material (Plexiglass) found in ingredient used.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2022· Albanese Confectionery Group, Inc.

Recalled Item: Albanese Dark Chocolate Espresso Bean packaged into 9oz plastic tubs...

The Issue: Undeclared Allergen - Peanut

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 9, 2022· Becton Dickinson & Co.

Recalled Item: BD Synapsys Microbiology Informatics Solution Recalled by Becton Dickinson &...

The Issue: When updating BD Kiestra customers to BD Synapsys version 4.10, the custom...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2022· Roche Diabetes Care, Inc.

Recalled Item: RocheDiabetes Care Platform Software version 2.5.2 material number...

The Issue: Potential for patient data mismatch when using browser "back" button to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2022· Acumed LLC

Recalled Item: 4.0mm x 10mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...

The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...

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

Class II — Potential Health HazardOngoing