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 31181–31200 of 49,976 recalls
Recalled Item: Philips Healthcare Ingenuity Core128 X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity CT X-Ray Recalled by Philips Electronics North...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: An error in NVIDIA GPU (Graphics Processing Unit) card drivers can occur for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance iCT X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Strata II / Strata NSC Valves (includes Burr Hole Recalled by...
The Issue: Medtronic Neurosurgery initiated a recall after receiving five (5) Product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Duodenoscope These instruments are intended to provide optical...
The Issue: Pentax initiated a field correction/safety alert for two (2) models of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (4.5...
The Issue: A portion of this lot of blood collection tubes was manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 12 Defibrillator/Monitor with End-Tidal CO2 option. The device is...
The Issue: The End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use...
The Issue: The End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXAMETHASONE ELIXIR Recalled by Vintage Pharmaceuticals LLC dba Qualitest...
The Issue: Failed Impurities/ Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Taclonex (calcipotriene and betamethasone dipropionate) Topical Suspension...
The Issue: Labeling: Incorrect or missing package insert: the affected product was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway Recalled by...
The Issue: Labeling error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morning Life Recalled by Won Industry Co. Due to Distribution of unapproved...
The Issue: Distribution of unapproved devices with incorrect air compression level setup
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compressible Limb Therapy System (Leg Cuffs Recalled by Won Industry Co. Due...
The Issue: Distribution of unapproved devices with incorrect air compression level setup
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.