Riverpoint Medical recalls Velosorb 4/0 undyed 18" absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have product number SV496G and lot number 20052721FX.
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 is non-sterile. This could lead to surgical site infections and increase the risk of complications during procedures.
The suture is non-sterile, meaning it does not meet the required cleanliness standards for surgical use. This can compromise the sterile field during procedures, potentially leading to infections at the surgical site. The risk is higher when the suture is used in wounds that require only short-term support.
Surgical professionals and patients who have purchased or received the Velosorb 4/0 undyed 18" suture with product number SV496G and lot number 20052721FX are affected. Those using the suture for skin and mucosal wounds are most at risk.
Check for the product number SV496G and lot number 20052721FX on the suture packaging. The suture is labeled as 'Velosorb 4/0 Undyed 18" P-12 Cutting' for soft tissue wounds.
Look for the product number SV496G and lot number 20052721FX on the suture packaging.
No, the suture is non-sterile and may cause surgical site infections, so it should not be used in surgical procedures.
The recall does not specify a remedy, so you should check with your healthcare provider or contact Riverpoint Medical for guidance.
Yes, it is intended for soft tissue approximation of skin and mucosa where only 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-0025-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0025-2021 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.
