Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Teleflex MEDICAL WECK Visistat 35. Used for the external skin Recalled by Teleflex Medical Due to Some boxes are labeled as Visistat Wide devices,...
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 Teleflex Medical directly.
Affected Products
Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.
Quantity: 12 units
Why Was This Recalled?
Some boxes are labeled as Visistat Wide devices, when in fact the contain Visistat Regular devices. The 6 individually packaged units within the boxes are correctly labeled.
Where Was This Sold?
This product was distributed to 1 state: KS
About Teleflex Medical
Teleflex Medical has 204 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report