Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NuStat 8" x12" Trauma Pad XR Hemafiber Recalled by Beeken Biomedical, LLC Due to Endotoxin levels exceeded allowable limits.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Beeken Biomedical, LLC directly.
Affected Products
NuStat 8" x12" Trauma Pad XR Hemafiber, 5-pack. For temporary control of internal organ space bleeding REF: XR-0812-5
Quantity: 15 units
Why Was This Recalled?
Endotoxin levels exceeded allowable limits.
Where Was This Sold?
This product was distributed to 1 state: MO
About Beeken Biomedical, LLC
Beeken Biomedical, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report