Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,082 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,082 in last 12 months

Showing 13801–13820 of 29,188 recalls

Medical DeviceJune 12, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection...

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· Becton Dickinson & Company

Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 65 Units Blood Collection...

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 dBC 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: Artis zee multi 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: Artis zeego 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: Artis zee floor 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 BA 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: Artis zee biplane 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) 68 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 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 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis dTA 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 Lithium HeparinN 75 USP Units Blood Collection Tubes Recalled...

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 dTC 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 Lithium HeparinN (LH) 158 USP Units 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· Beckman Coulter Inc.

Recalled Item: SYNCHRON Systems Barbiturates Reagent (BARB 1 X 250) Recalled by Beckman...

The Issue: The firm has identified that cross-reactivity testing may not meet the...

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· 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