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. 2,747 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,747 in last 12 months

Showing 47414760 of 53,528 recalls

Medical DeviceAugust 20, 2024· Cypress Medical Products LLC

Recalled Item: BinaxNOW Respiratory Strep A Test Kit Recalled by Cypress Medical Products...

The Issue: Due to a classification error in our inventory management system, these...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2024· Cypress Medical Products LLC

Recalled Item: Acceava Respiratory Strep A Recalled by Cypress Medical Products LLC Due to...

The Issue: Due to a classification error in our inventory management system, these...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: Custom Inflation Kit Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixSKY Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: MONARCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: DiamondTOUCH Digital Inflation Device Recalled by Merit Medical Systems,...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: BlueFIRE Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: Blue Diamond Digital Inflation Device Recalled by Merit Medical Systems,...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: StabiliT TOUCH Syringe Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: IntelliSystem Inflation Device Recalled by Merit Medical Systems, Inc. Due...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Hologic Inc

Recalled Item: Selenia Dimensions/ 3Dimensions-Digital breast tomosynthesis Software...

The Issue: Identified an issue with Selenia Dimensions 1.12.0 and 3Dimensions 2.3.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil Tray that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Septo Pack that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical T and A Pack that contains Recalled by Windstone Medical...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil Pack that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil ENT Pack that contains the Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
FoodAugust 15, 2024· Refresco Beverages US Inc

Recalled Item: Great Value Recalled by Beverages US Inc Due to Product contains inorganic...

The Issue: Product contains inorganic arsenic above action level set in industry...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2024· Biocompatibles UK, Ltd.

Recalled Item: Varithena (polidocanol injectable foam) Administration Pack Recalled by...

The Issue: Defective Delivery System: incorrect silicone oil-free NormJect 10 mL Luer...

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

Class III — Low RiskOngoing
Refund