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. 2,681 recalls have been distributed to Oklahoma in the last 12 months.
Showing 821–840 of 28,654 recalls
Recalled Item: BD Pyxis Pro MedStation Main Recalled by CareFusion 303, Inc. Due to...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various models of BD Pyxis MedFlex Recalled by CareFusion 303, Inc. Due to...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various models of BD Pyxis Pro 7-Drawer Auxiliary Recalled by CareFusion...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...
The Issue: There is a potential safety issue associated with the magnet venting paths...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...
The Issue: There is a potential safety issue associated with the magnet venting paths...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Serial Numbers/BD Pyxis CII Safe ES Tower Main Recalled by CareFusion...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various models of BD Pyxis Medbank: numbers: 1137-00 1145-00 Recalled by...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET...
The Issue: The potential for micro-air bubbles observed in the bloodline and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog...
The Issue: Due to manufactured products that deviated from established specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog...
The Issue: Due to manufactured products that deviated from established specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving...
The Issue: Due to manufactured products that deviated from established specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog...
The Issue: Due to manufactured products that deviated from established specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AART Pectoral Implant Product Name: Pectoral Implant...
The Issue: Due to manufactured products that deviated from established specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AART Gluteal Implant Product Name: Gluteal Implant Model/Catalog...
The Issue: Due to manufactured products that deviated from established specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T-FILL End Caps for SAFE-T-FILL Blood Gas Capillaries Recalled by ASP...
The Issue: Due to products manufactured under an inadequate quality system to include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....
The Issue: Due to products manufactured under an inadequate quality system to include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....
The Issue: Due to products manufactured under an inadequate quality system to include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T-FILL MicroHematocrit Capillary Tubes Recalled by ASP Global, LLC. dba...
The Issue: Due to products manufactured under an inadequate quality system to include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....
The Issue: Due to products manufactured under an inadequate quality system to include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....
The Issue: Due to products manufactured under an inadequate quality system to include...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.