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. 2,576 recalls have been distributed to Oklahoma in the last 12 months.
Showing 17061–17080 of 49,976 recalls
Recalled Item: Philips Respironics V60 Ventilator Part Number 1053614 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1076716 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1137292 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1076717 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number R1053618 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V680 Ventilator Part Number 850011 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1138747 - Product...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1137276 - Product...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1053616 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1053617 - Product Usage:...
The Issue: Potential issues with ventilator navigation ring interface and liquid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bone fixation nail. TRIGEN INTERTAN - Product Usage: indicated for Recalled...
The Issue: Manufacturing packaging error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassChrom Amino Acid Analysis Plasma Control Level I Recalled by...
The Issue: Products do not meet stability criteria and may impact results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3PLUS1 Multilevel Plasma Calibrator Set Recalled by Chromsystems Instruments...
The Issue: Products do not meet stability criteria and may impact results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassChrom Amino Acid Analysis Plasma Control Level III Recalled by...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassChrom Amino Acid Analysis Plasma Control Level II Recalled by...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mesalamine Delayed-Release Tablets Recalled by AVKARE Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.