Riverpoint Medical recalls Velosorb 4/0 undyed 30" absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have Product Number SV426 and UDI 20884521151731.
The surgical suture is non-sterile. Use could compromise the sterile field, increase risk of a surgical site infection, and increase break strength retention.
Riverpoint Medical is recalling Velosorb Fast Braided Absorbable Suture because it's non-sterile. Using this suture in surgery could lead to infections or complications since it's not designed to maintain sterility during procedures.
The suture is non-sterile, meaning it doesn't meet surgical standards for cleanliness. This can compromise the sterile field during procedures, increasing the chance of infections at the surgical site. It also affects the suture's ability to hold together without breaking over time.
Surgical professionals who use the Velosorb suture for skin and mucosal wounds. Those using the product for procedures requiring only 7-10 days of wound support are most at risk.
Check for Product Number SV426 and Unique Device Identifier (UDI) 20884521151731 on the packaging. The suture is used for soft tissue approximation where only 7-10 days of wound support is needed.
Look for Product Number SV426 and UDI 20884521151731 on the suture packaging.
No, the suture is non-sterile and not intended for use in procedures requiring sterility, such as ligation or specialized surgeries.
The recall record does not specify a remedy, so you should check with your supplier or healthcare provider for guidance.
The recall states it increases risk of surgical site infections but does not mention serious injury mechanisms like lacerations or fires.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0012-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0012-2021 from Riverpoint Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
