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. 2,609 recalls have been distributed to Oklahoma in the last 12 months.
Showing 13161–13180 of 28,654 recalls
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: 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: 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: Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Recalled...
The Issue: Due to low Quality Control recovery and invalid Calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and...
The Issue: The firm received a report of an atypical dataset being generated. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Users may experience intermittent slide dispense issues with some cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS chemistry Products K+ Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Users may experience intermittent slide dispense issues with some cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rosa Brain 3.0 Recalled by MEDTECH SAS Due to The instrument holder may be...
The Issue: The instrument holder may be sent on a trajectory that is not within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Users may experience intermittent slide dispense issues with some cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1400-04. For Recalled...
The Issue: Some Thorecon disposable tensioners supplied in different Plating System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1700-10. For Recalled...
The Issue: Some Thorecon disposable tensioners supplied in different Plating System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1200-08. For Recalled...
The Issue: Some Thorecon disposable tensioners supplied in different Plating System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1500-04-S. For...
The Issue: Some Thorecon disposable tensioners supplied in different Plating System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1300-04-S. For...
The Issue: Some Thorecon disposable tensioners supplied in different Plating System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...
The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE Recalled by Medline Industries...
The Issue: The recall is being conducted due to a potential defective component on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embryology Heated Plate within the RI Witness Recalled by CooperSurgical,...
The Issue: The touchpad may not work properly after cleaning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron Systems Opiate 2000 ng Reagent (OP2 1 x 250) Recalled by Beckman...
The Issue: Cross-reactivity testing may not meet the claims indicated in the Opiate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opiate 300 Ng Reagent (OP 1 X 250) for use Recalled by Beckman Coulter Inc....
The Issue: Cross-reactivity testing may not meet the claims indicated in the Opiate 300...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...
The Issue: It is possible that the forced electron density settings will be changed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.