Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units 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 Velosorb Fast Braided Absorbable Suture because it's non-sterile. Using this suture during surgery could lead to infections or complications in the surgical site.
The suture is non-sterile, meaning it lacks the required cleanliness for surgical use. This can compromise the sterile field during surgery, potentially increasing the risk of infection at the surgical site. The suture is designed for short-term wound support (7-10 days), so the risk is lower than for longer-term uses.
Surgical professionals who use this specific suture product are affected. The risk is low for most procedures since the suture is intended for short-term wound support.
Check for the UDI number 20884521151755 and lot number 20061504FX on the suture packaging. This specific product is intended for soft tissue approximation in short-term wound support.
Look for the UDI number 20884521151755 and lot number 20061504FX on the suture packaging to confirm if it's affected.
No, this suture is non-sterile and intended only for specific surgical procedures where short-term wound support is needed (7-10 days). It should not be used for ligation or in sensitive areas like eyes, heart, or nerves.
The recall does not specify a remedy, so you should check the packaging for the UDI and lot number to confirm if it's affected. If it is, contact Riverpoint Medical for further instructions.
The recall states it's non-sterile, which could increase infection risk but does not mention causing serious injury. The hazard level is low risk as it's designed for short-term use.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0048-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0048-2021 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.
