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. 2,647 recalls have been distributed to Oklahoma in the last 12 months.
Showing 6721–6740 of 28,654 recalls
Recalled Item: Titan Touch NB Scrot Zero 16cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shanghai United Imaging Healthcare Co. Recalled by Shanghai United Imaging...
The Issue: Due to a software issue where the process of patient scanning, the scatter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Infr Zero Ang 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromic Gut Absorbable Sutures Recalled by Covidien, LP Due to Medtronic was...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Infr Zero 16cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 0-Deg Infrapubic 20 Cm Recalled by Coloplast Manufacturing US, LLC Due...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plain Gut Absorbable Sutures Recalled by Covidien, LP Due to Medtronic was...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Infr Zero Ang 22cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 0-Deg Scrotal 22 Cm Recalled by Coloplast Manufacturing US, LLC Due to...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mild Chromic Gut Absorbable Sutures Recalled by Covidien, LP Due to...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Infr Zero 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 0-Deg Scrotal 18 Cm Recalled by Coloplast Manufacturing US, LLC Due to...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Pump Recalled by Coloplast Manufacturing US, LLC Due to A...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan NB Infra Zero Ang 16cm Recalled by Coloplast Manufacturing US, LLC Due...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIOX NX19 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...
The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4...
The Issue: Not able to achieve desired pressure and not holding pressure result from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4...
The Issue: Not able to achieve desired pressure and not holding pressure result from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4...
The Issue: Not able to achieve desired pressure and not holding pressure result from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIOX FX25 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...
The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIOX RX15 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...
The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.