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. 2,642 recalls have been distributed to Oklahoma in the last 12 months.
Showing 8861–8880 of 28,654 recalls
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott HeartMate Touch Communication System Recalled by Thoratec Corp. Due...
The Issue: If LVAS communication system is trying to establish Bluetooth connection and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Ocean Water Seal Chest Drain is a plastic Recalled by Atrium Medical...
The Issue: Inadequate/inappropriate Set-Up Instructions, which may result in delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalys Precision Laser System Recalled by AMO Manufacturing USA, LLC Due to...
The Issue: Aberrometer and precision laser systems are affected by a remote code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iDesign Recalled by AMO Manufacturing USA, LLC Due to Aberrometer and...
The Issue: Aberrometer and precision laser systems are affected by a remote code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of Recalled...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of Recalled...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of...
The Issue: Balloon pinhole results in losss pressure or fails to gain or maintain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...
The Issue: If the system experiences an overvoltage / power surge it can cause a short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system Recalled...
The Issue: If the system experiences an overvoltage / power surge it can cause a short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomeme SARS-CoV-2- Real Time RT-PCR Test Recalled by Biomeme, Inc. Due to...
The Issue: The current IFU specifies a shelf-life of one week after resuspension of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen ceiling with software VD12-angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen floor with software VD12-angiography systems developed for...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aspiration Syringe Kit Recalled by MICROVENTION INC. Due to Syringe Kits...
The Issue: Syringe Kits labeled for distribution OUS were inadvertently shipped to US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q ceiling with software VD12-angiography systems developed for single...
The Issue: If SID (source-to-image distance) lift movement is activated and x-ray shall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.