Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 18" Recalled by Riverpoint Medical, LLC Due to The surgical suture is non-sterile. Use could compromise...
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 Riverpoint Medical, LLC directly.
Affected Products
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 18" P-24, Product Number: SV9911G, UDI: 20884521149776 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.
Quantity: 1258
Why Was This Recalled?
The surgical suture is non-sterile. Use could compromise the sterile field, increase risk of a surgical site infection, and increase break strength retention.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Riverpoint Medical, LLC
Riverpoint Medical, LLC has 47 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report