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. 2,083 recalls have been distributed to Oklahoma in the last 12 months.
Showing 5321–5340 of 28,654 recalls
Recalled Item: Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) Recalled by...
The Issue: Use of a 1.4 drill in hard bone conditions caused increased insertion forces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use only....
The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRAPHENANO DENTAL G-CAM Recalled by GRAPHENANO DENTAL SL Due to Machining...
The Issue: Machining error on cams renders the device unusable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Select Cycler Recalled by Fresenius Medical Care Holdings, Inc. Due...
The Issue: Affected Liberty Select cyclers may display an incorrect time stamp on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...
The Issue: The efficacy of the manual cleaning process cannot be assured for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...
The Issue: The efficacy of the manual cleaning process cannot be assured for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...
The Issue: The efficacy of the manual cleaning process cannot be assured for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...
The Issue: The efficacy of the manual cleaning process cannot be assured for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...
The Issue: The efficacy of the manual cleaning process cannot be assured for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX Recalled by Philips North America Llc Due to Potential...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Initial System Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Power/Pulsar Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips North America Llc Due to Potential component...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Processing Module The Alinity c Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 Processing Module 02P24-02 02P24-40 01R24-56 01R25-56...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Blood Analysis System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed a potential issue that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.