Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,510 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,510 in last 12 months

Showing 1324113260 of 27,462 recalls

Medical DeviceJune 12, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer LH (Lithium Heparin) 102 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· Becton Dickinson & Company

Recalled Item: BD Vacutainer PST Blood Collection Tubes Recalled by Becton Dickinson &...

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 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· Becton Dickinson & Company

Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 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· 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: Artis zee floor MN 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 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· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis FA 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 dMP 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 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 ceiling 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 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 dFA 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 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· 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· 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 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: 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 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