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. 2,520 recalls have been distributed to Oklahoma in the last 12 months.
Showing 20761–20780 of 49,976 recalls
Recalled Item: Vitamin 9 Lyophilized Recalled by KRS Global Biotechnology, Inc Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alpha Lipoic Acid (PF) 750 mg/30 mL (25 mg/mL) 30 mL Single Dose Vial for IV...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zarontin (ethosuximide capsules Recalled by Pfizer Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The expiry date on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ethosuximide capsules Recalled by Pfizer Inc. Due to Labeling: Incorrect or...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The expiry date on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine in 0.9% Sodium Chloride (PF) Recalled by KRS Global...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System -...
The Issue: Berkeley Disposa-Filter may possess an insufficient ultrasonic weld defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cerelink ICP Monitor Recalled by Integra LifeSciences Corp. Due to There is...
The Issue: There is a potential for a progressive decline in observed ICP readings of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sheath Introducer Kit - Product Usage: intended Recalled by Merit...
The Issue: labeling error: Due to a manufacturing issue, product package was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNI Hip System Model Recalled by OMNIlife science Inc. Due to Stems missing...
The Issue: Stems missing porous coating on the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respironics V680 Ventilator Recalled by Respironics California, LLC Due to...
The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Transducer (M2736A) Recalled by Pacific Medical Group Inc. Due to...
The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button-Style Tocotransducer (Nautilus) Recalled by Pacific Medical Group...
The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toco+ transducer with ECG/IUP capability (wired) Recalled by Pacific Medical...
The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respironics RP-UI Assy Recalled by Respironics California, LLC Due to...
The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External Toco Transducer (M1355A) Recalled by Pacific Medical Group Inc. Due...
The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respironics RP-Touch Screen Recalled by Respironics California, LLC Due to...
The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loop-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...
The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toco M2734A Recalled by Pacific Medical Group Inc. Due to Fetal/maternal...
The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 -...
The Issue: Due to low Quality Control recovery and invalid Calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respironics V60 Ventilator Recalled by Respironics California, LLC Due to...
The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.