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. 1,978 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,978 in last 12 months

Showing 1576115780 of 29,228 recalls

Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TK CONT EPIDURALTUOHY Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CNB400TU3KUE 18GX4 CONTI THY ULTRA 360 Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TKFSA FULL TRAY W/17G TUOHY 19G SPRW Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE18TOD CONT EPIDURAL TRAY LF Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CLAMP STYLE CATH. CONNECTOR 18-19 GA- LF Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TOD CONT EPIDURAL TRAY LF Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TKFPS PERIFIX FX CONT. EPID TRAY-LF Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: GOVCE18TK ACCU-BLOC PERIFIX KIT Recalled by B. Braun Medical, Inc. Due to...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TKFMHDT 17 GA X 4 FULL EPID KIT Recalled by B. Braun Medical, Inc. Due...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TB19C CONT EPIDURAL TRAY Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Thread PLGA Full Thread Interference Screw Recalled by Zimmer Biomet,...

The Issue: The Gentle Thread PLGA Round Head, 7x20mm and the Gentle Thread PLGA Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Thread PLGA Round Head Interference Screw Recalled by Zimmer Biomet,...

The Issue: The Gentle Thread PLGA Round Head, 7x20mm and the Gentle Thread PLGA Full...

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 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 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 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