Riverpoint Medical recalls non-sterile Velosorb 2/0 suture to prevent surgical infections. Affected items have specific UDI and lot numbers.
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 non-sterile Velosorb fast braided absorbable sutures. Using these sutures in surgery could lead to infections or complications because they aren't sterile.
The suture is non-sterile, meaning it lacks the required cleanliness for surgical use. This can compromise the sterile field during surgery, increasing the chance of infection. It also affects the suture's ability to hold together properly over time.
Surgical professionals who use the recalled Velosorb sutures for skin and mucosal repairs. Patients undergoing procedures with these sutures are at risk of infection.
Check for the product name 'Velosorb 2/0 Undyed 30" GS-20 CV9975G' with UDI 20884521149585. The lot number is 20060930X.
Look for the UDI number 20884521149585 and lot number 20060930X on the suture packaging.
No, the suture is non-sterile and not intended for surgical use without proper sterilization.
The recall does not specify a remedy, so check with your healthcare provider for guidance.
Look for the UDI number 20884521149585 and lot number 20060930X on the suture packaging.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0045-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0045-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.