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. 2,509 recalls have been distributed to Oklahoma in the last 12 months.
Showing 22021–22040 of 49,976 recalls
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: 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.
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.
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 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: 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: 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: 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: 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: 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: Hydromorphone HCl in 0.9% sodium chloride Recalled by PharMEDium Services,...
The Issue: Incorrect Product Formulation; Firm's customer resource center (CRC)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Myorisan (isotretinoin capsules Recalled by Akorn Inc Due to Labeling: Label...
The Issue: Labeling: Label mix-up: Product secondary carton erroneously states 40mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PTS Panels Lipid Panel test strip: IVD Lipid Panel Test Recalled by Polymer...
The Issue: The MEMo chips provided with lot P901 may be mislabeled, the MEMo Chip may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Panels Lipid Panel test strip: IVD Lipid Panel Recalled by...
The Issue: The MEMo chips provided with lot P901 may be mislabeled, the MEMo Chip may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Overlap Vest Recalled by Burlington Medical, LLC Due to The protective...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vest Recalled by Burlington Medical, LLC Due to The protective material used...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontal Apron with Quick Drop Velcro Closure (no elastic) Recalled by...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hood Recalled by Burlington Medical, LLC Due to The protective material used...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontal Apron Velcro Closure Recalled by Burlington Medical, LLC Due to The...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontal Support Belt Apron Recalled by Burlington Medical, LLC Due to The...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.