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. 2,565 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,565 in last 12 months

Showing 2292122940 of 53,528 recalls

Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis dBA Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis TC Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer LH (Lithium Heparin) 34 I.U. Plus Blood Collection Tubes...

The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis dFC Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis TA Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2019· Randox Laboratories, Limited

Recalled Item: Human Assayed Multi-Sera Level 2 Recalled by Randox Laboratories, Limited...

The Issue: The RX Series control target and range value for ALT (Tris buffer without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Olympus Corporation of the Americas

Recalled Item: Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm...

The Issue: WM-NP/DP2 workstations could become unstable and may fall over if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity ci -series System Control¿Module Recalled by Abbott Gmbh & Co. KG...

The Issue: Abbott has identified an issue with all on market versions (v2.6.0 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to An...

The Issue: An issue with the handcontroller may result in either spontaneous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView SPECT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: An issue with the handcontroller may result in either spontaneous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to An...

The Issue: An issue with the handcontroller may result in either spontaneous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only)...

The Issue: Lack of an adequate sterilization validation.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only)...

The Issue: Lack of an adequate sterilization validation.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Molded Products Inc

Recalled Item: Luer Lock Set - Catalog # MPC-125 Recalled by Molded Products Inc Due to...

The Issue: Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Porta Shield Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: 2 pc Full Wrap Vest & Kilt Back-Saver Recalled by Burlington Medical, LLC...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Kilt Recalled by Burlington Medical, LLC Due to The protective material used...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Thyroid Collar Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Thyroid Collar Oversize Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Sleeve Recalled by Burlington Medical, LLC Due to The protective material...

The Issue: The protective material used in the manufacture of the products could...

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

Class II — Potential Health HazardOngoing