Riverpoint Medical recalls Velosorb 3/0 undyed suture due to non-sterile condition, which may cause surgical site infections. Affected units have Product Number SV935 and UDI 20884521151755.
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. This could lead to surgical site infections and increased risk of infection during procedures.
The suture is non-sterile, meaning it doesn't meet surgical cleanliness standards. This can compromise the sterile field during procedures, increasing the chance of infection at the surgical site.
Surgical professionals and patients who used the recalled Velosorb suture for soft tissue approximation. Those with the Product Number SV935 and UDI 20884521151755 are most at risk.
Check for Product Number SV935 and UDI 20884521151755 on the suture packaging. The suture is intended for soft tissue approximation where 7-10 days of wound support is needed.
Look for Product Number SV935 and UDI 20884521151755 on the suture packaging to confirm if it's affected.
No, this suture is non-sterile and intended only for soft tissue approximation where 7-10 days of wound support is needed. It should not be used for ligation, ophthalmic, cardiovascular, or neurological procedures.
Using non-sterile suture can compromise the sterile field, increase risk of surgical site infections, and affect break strength retention.
Check for Product Number SV935 and UDI 20884521151755 on the suture packaging. The suture is intended for soft tissue approximation where 7-10 days of wound support is needed.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0011-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0011-2021 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.
