Reported Jun 20, 2018 · Terminated
Part #: SAM XT-C, Model: Hi-Viz Blue
The Seaberg Company Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: The Seaberg Company Inc · 27350 SW 95th Ave Ste 3038 · Wilsonville, OR · 97070-7709
Is this the product you have?
- Part #: SAM XT-C
- ModelHi-Viz Blue
- Lot codes and dates
Lot #: XT1808XT1809XT1810
- Amount recalled
- N/A
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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