Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,630 recalls have been distributed to Delaware in the last 12 months.
Showing 9681–9700 of 48,330 recalls
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: Instructions for Use for the following Leksell Stereotactic System and...
The Issue: The incorrect IFU was distributed with the devices.
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: Trilogy Evo O2 and LifeVentEVO2 Portable Electric Ventilator Recalled by...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 0-Deg Scrotal 20 Cm Recalled by Coloplast Manufacturing US, LLC Due to XXX
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Step Bladeless Trocars Recalled by Covidien, LP Due to Medtronic was made...
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 Scro Zero Ang 20cm 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 Touch Scro 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: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4...
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 34X4...
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: Titan Touch NB Scrot 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: Trilogy Evo Universal Portable Electric Ventilator Recalled by Philips...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan NB Scrotal 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: Titan Pump Assembly 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: Trilogy EV300 Portable Electric Ventilator Recalled by Philips Respironics,...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
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.
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: 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: 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 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.