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Beeken Biomedical, LLC recalls NuStat 8" x12" Trauma Pad XR Hemafiber, 5-pack. For temporary control of internal organ space bleeding REF: XR-0812-5
Recalled December 8, 2021 · FDA recall Z-0309-2022 · Beeken Biomedical
Hazard
Endotoxin levels exceeded allowable limits. · FDA Class II
Units
15 units
Sold at
US in the state of MO
Description
Endotoxin levels exceeded allowable limits.
Product
NuStat 8" x12" Trauma Pad XR Hemafiber, 5-pack. For temporary control of internal organ space bleeding REF: XR-0812-5
Manufacturer(s)
Beeken Biomedical, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →