Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which can cause surgical site infections. Affected units have UDI 20884521151021. Stop using immediately to prevent infection risks.
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 sutures because they are non-sterile. Using these sutures during surgery could lead to infections or complications. This is a serious risk for surgical procedures.
The suture is non-sterile, meaning it lacks the required cleanliness for surgical use. This can compromise the sterile field during procedures, increasing the chance of infections. It also affects the suture's ability to hold together without breaking.
Surgical professionals and hospitals using the recalled Velosorb 3/0 suture (UDI: 20884521151021) are most at risk. Patients undergoing surgery with this suture could face infection risks.
Check for the UDI code 20884521151021 on the suture packaging. The product is a Velosorb 3/0 undyed 30" C-13 cutting suture with lot number 20061715FX.
Discard the non-sterile suture to prevent infection risks during surgery.
No, this suture is not sterile and should not be used in surgical procedures. It is intended only for specific soft tissue applications where 7-10 days of support is needed.
Discard the suture immediately to avoid infection risks. Do not use it in any surgical procedure.
Look for the UDI code 20884521151021 on the suture packaging. The lot number is 20061715FX.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0049-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0049-2021 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.
