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. 2,571 recalls have been distributed to Oklahoma in the last 12 months.
Showing 15841–15860 of 28,654 recalls
Recalled Item: MAYFIELD Infinity XR2 Base Unit-Extended Recalled by Integra LifeSciences...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT Recalled by Integra LifeSciences...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD INFINITY XR2 BASE UNIT Recalled by Integra LifeSciences Corp. Due...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT Recalled by Integra LifeSciences...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250/MEVION S250i Proton Beam Radiation therapy system Product Usage:...
The Issue: QFix has advised Mevion Medical Systems that they are identifying...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation stand-alone software treatment planning system Recalled by...
The Issue: If the beam model has a highly asymmetric primary source, it is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is Recalled...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quasar MD Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 Recalled by...
The Issue: An incorrect control board and firmware installed in some of the Hand Held...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3D TOP Ceiling Stand Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: In rare cases of insufficient maintenance or high clinical workload, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Neonatal Flow Sensor Cable used on devices CARESCAPE R860 Recalled by...
The Issue: The Neonatal Flow Sensor Cable may be missing the connector housing exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...
The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Gantry rotation or...
The Issue: Gantry rotation or proton irradiation can be allowed even if apertures or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based...
The Issue: The margin tool in Leksell GammaPlan 11.1 systematically overestimates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.