The Seaberg Recalls
3 recalls on record · June 20, 2018 to June 20, 2018 · Medical Devices
June 20, 2018Medical DevicesFDA
The Seaberg Company Inc recalls Part #: SAM XT-C, Model: Hi-Viz Blue
Hazard: Based on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human patient to stop arterial blood flow. There is a remote chance that a serious injury and/or death could occur as a result of the failure of the device.
June 20, 2018Medical DevicesFDA
The Seaberg Company Inc recalls Part #: SAM XT-C, Model: Hi-Viz Orange or Civilian
Hazard: Based on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human patient to stop arterial blood flow. There is a remote chance that a serious injury and/or death could occur as a result of the failure of the device.
June 20, 2018Medical DevicesFDA
The Seaberg Company Inc recalls Part #: SAM XT-M, Model: Tactical Black or Military
Hazard: Based on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human patient to stop arterial blood flow. There is a remote chance that a serious injury and/or death could occur as a result of the failure of the device.