Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,464 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,464 in last 12 months

Showing 2184121860 of 50,117 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· 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 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· 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: 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· Becton Dickinson & Company

Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 126 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 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 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: 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 Lithium HeparinN (LH) 95 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 11, 2019· Life Technologies Corporation

Recalled Item: CTSTM Essential 8 Medium Recalled by Life Technologies Corporation Due to...

The Issue: Component was not tested by the supplier for adventitious agents

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 11, 2019· Life Technologies Corporation

Recalled Item: StemPro¿ MSC SFM CTS" Recalled by Life Technologies Corporation Due to...

The Issue: Component was not tested by the supplier for adventitious agents

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· 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 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· 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· 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