NuStat 8" x12" Trauma Pad XR Hemafiber, 5-pack. For temporary control of internal organ space bleeding REF: XR-0812-5
FDA Recall Z-0309-2022 · Posted None
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Recalling FirmBeeken Biomedical, LLC
Recall StatusOpen, Classified
Product CodePOD
Date Initiated2021-10-14
Product Quantity15 units
Reason for Recall
Endotoxin levels exceeded allowable limits.
Firm Action
Beeken initiated notification via e-mail on October 14, 2021 and follow-up Urgent Medical Device Voluntary Recall Notification Letter, Certified mail dated October 20, 2021. Letter states reason for recall, health risk and action to take:
Immediately check your inventory and quarantine all NuStat 8"x12" Trauma Pad XR-0812-5
Hemostatic Dressing (Lot Code: 20C015) to prevent further use.
" Ensure relevant staff members, including clinicians, surgeons, OR staff and product return staff
are informed of this recall.
" If you have supplied any NuStat 8"x12" Trauma Pad XR-0812-5 Hemostatic Dressing (Lot Code:
20C015) to any other organization or clinical site, please advise that organization of this recall
and notify Beeken Biomedical of that organization's name, address, and contact person so that
we may contact them immediately.
" Please immediately complete the attached Acknowledgement form - even if you have none of
this product- and return the form to Beeken Biomedical by email to:
[email protected] or by mail to
Recall Administrator
Beeken Biomedical, LLC
378 Page Street, Suite 201
Stoughton, MA 02072
questions about this recall, please email or phone Beeken Biomedical
Customer Service at 888-497-7376, Monday through Friday, between the hours of 8:30 am
and 4:00 pm (EST) or otherwise leave a message which will be returned on the next working day.
Root Cause
Under Investigation by firm
Distribution Pattern
US in the state of MO
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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