Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which could increase surgical site infections. Affected units have UDI 20884521150918.
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. This could lead to surgical site infections during procedures and compromise the sterile field. Patients using this suture should stop using it and contact the manufacturer.
The suture is non-sterile, meaning it doesn't meet surgical cleanliness standards. This increases the chance of infection at the surgical site and could weaken the suture's ability to hold together over time.
Healthcare professionals using the suture for soft tissue procedures are affected. Those with the specific UDI number 20884521150918 are most at risk.
Check for the UDI number 20884521150918 on the product label. The suture is labeled as 'Covidien Velosorb 3/0 Undyed 30" CV-25 Taper CV3110' for soft tissue procedures.
Look for the UDI number 20884521150918 on the suture packaging or label.
No, this suture is non-sterile and intended only for soft tissue procedures where 7-10 days of wound support is needed. It should not be used for ligation or sensitive areas like eyes or blood vessels.
The recall does not specify a remedy, so contact Riverpoint Medical directly for guidance on disposal or replacement.
The recall states it could increase infection risk but does not mention serious injury. The hazard level is low risk due to the non-sterile condition.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0047-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0047-2021 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.
