Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due to The recall was initiated because Superstat Corporation has...
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 Superstat Corp directly.
Affected Products
Superstat Modified Collagen Hemostatic Sponge, 4x4 Pledget, 3.0%, Part# 9102-00. For use when hemostasis is desired along suture lines, in diffusely bleeding sites, in incisions, dissections, and around arterial or venous anastomoses. Indicated in oozing bleeding, either capillary or venous, in almost all types of incisions or wounds, and as an adjunct to conventional closure techniques
Quantity: 26,422 units
Why Was This Recalled?
The recall was initiated because Superstat Corporation has confirmed that no documentation are available to verify that quarterly dose sterility audits were performed for the Superstat Modified Collagen Hemostatic Sponge.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Superstat Corp
Superstat Corp has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report