Seaberg recalls Hi-Viz Blue tourniquets (SAM XT-C) due to potential stitch failure that could stop blood flow, risking serious injury or death during medical use. Affected units include specific lots.
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.
Seaberg is recalling Hi-Viz Blue tourniquets (SAM XT-C model) because internal testing found stitches securing the buckle to the belt might fail, potentially stopping blood flow during medical use. This could lead to serious injury or death in rare cases.
The tourniquet's stitches could fail while in use, stopping blood flow to a patient's limb. This failure could cause serious injury or death if it occurs during medical procedures.
Healthcare professionals using the tourniquet on patients are most at risk. Patients receiving medical treatment with this device may also be affected.
Check for the SAM XT-C model with Hi-Viz Blue color. Affected units have lot numbers XT1808, XT1809, or XT1810.
Immediately stop using the tourniquet if it has the SAM XT-C model with Hi-Viz Blue color and affected lot numbers.
No, the recall states there is a remote chance of serious injury or death due to potential stitch failure.
Lot numbers XT1808, XT1809, and XT1810.
Check for the SAM XT-C model with Hi-Viz Blue color and lot numbers XT1808, XT1809, or XT1810.
We’ve drafted a message you can send Seaberg to request your refund or repair — edit it as you like.
Subject: Recall Z-2228-2018 — Seaberg Seaberg Hello, I own a Seaberg that is covered by recall Z-2228-2018 from Seaberg. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
