Riverpoint Medical recalls Velosorb 4/0 absorbable sutures due to non-sterile condition, which may cause surgical site infections. Affected units have specific lot numbers and UDI codes.
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. This could lead to infections during surgery or weaken the suture's ability to hold tissue together.
The suture is non-sterile, meaning it may not meet surgical cleanliness standards. This could increase the chance of infection at the surgical site and reduce the suture's ability to stay intact for the intended 7-10 days.
Surgical professionals and patients who have received the Velosorb 4/0 suture with lot number 20060928X or UDI 20884521151632 are affected. Those using the product for skin and mucosal wounds are most at risk.
Check for the lot number 20060928X or UDI code 20884521151632 on the product packaging. The suture is labeled for soft tissue approximation of skin and mucosa, not for ligation or specialized procedures.
Look for the lot number 20060928X or UDI code 20884521151632 on the suture packaging.
No, this suture is intended only for soft tissue approximation of skin and mucosa, not for ligation or specialized procedures like ophthalmic or cardiovascular surgery.
The recall does not specify a remedy, so check with your healthcare provider or the manufacturer for guidance.
Look for the lot number 20060928X or UDI code 20884521151632 on the product 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-0043-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0043-2021 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.
