Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,076 recalls have been distributed to Oklahoma in the last 12 months.
Showing 13641–13660 of 28,654 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: ZOLL AED PRO Automated External Defibrillator Product Usage: The AED...
The Issue: There is a potential for the device to fail to deliver energy to the patient.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
Recalled Item: VAMPIRO V5001-minimally invasive poole suction sleeve that is an accessory...
The Issue: Lack of package integrity may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.