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. 1,097 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,097 in last 12 months

Showing 15781–15800 of 29,228 recalls

Medical DeviceJuly 19, 2018· Trilliant Surgical, LLC

Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for...

The Issue: Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2018· Trilliant Surgical, LLC

Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for...

The Issue: Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2018· Trilliant Surgical, LLC

Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for:...

The Issue: Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT Creatine Kinase Recalled by Abbott Laboratories, Inc Due to...

The Issue: The product has a stability issue which may lead to an error code indicating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT Creatine Kinase Recalled by Abbott Laboratories, Inc Due to...

The Issue: The product has a stability issue which may lead to an error code indicating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 400 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 300 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 320 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 400 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 9 mm x 360 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 400 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 340 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 300 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 13 mm x 320 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 340 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 15 mm x 440 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 460 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 360 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 440 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 400 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing