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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 27041–27060 of 49,976 recalls
Recalled Item: Stanbio AC power adapter for the HemoPoint H2 meter Recalled by Stanbio...
The Issue: The US prong (type A) adapter plate may crack, break, or detach and remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Slice (Air) - Model no. 728246 Recalled by Philips Medical...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core - Model no. 728321 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fornier Phantom Fiber(TM) Sutures: Item Number Description SMB000425 4.5 MM...
The Issue: Data has shown that degradation of a raw material used in Phantom Fiber may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore (Radiology) - Model no. 728244 Recalled by Philips...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP Surgical Light Recalled by GETINGE US SALES LLC Due to The...
The Issue: The manufacturer received complaints indicating that the device's central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Recalled...
The Issue: Device may display a battery missing error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GloCyte RBC Reagent - Product Usage: The GloCyte Automated Cell Recalled by...
The Issue: RBC Reagent failure. High fluorescent counts during RBC Reagent + Diluent QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Nasal Solution (Nasal Spray) 0.1% (137 mcg per spray)...
The Issue: Sun Pharmaceutical is recalling Azelastine HCl Nasal Solution, 0.1% (30 mL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear Recalled by ICU...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14 cm (5.5") Appx 0.27 ml Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.