Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Zip 8i Surgical Skin Closure Device Recalled by Zipline Medical Due to The manufacturers seal may not be present on...
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 Zipline Medical directly.
Affected Products
Zip 8i Surgical Skin Closure Device; for incisions up to 8 cm. Product number PS2080 Indicated for use during and after skin incision procedures to approximate skin and hold together skin edges until healing can take place.
Quantity: 3109 - total - all model numbers
Why Was This Recalled?
The manufacturers seal may not be present on the Nylon pouch resulting in lack of assurance for sterility.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zipline Medical
Zipline Medical has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report