Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 992 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
992 in last 12 months

Showing 21421–21440 of 47,938 recalls

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 biplane 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: 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: 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· 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· 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: 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: 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 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· 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 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· 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 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· 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· 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· 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 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