Riverpoint Medical recalls Velosorb 5/0 absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have product number CV2293 and lot 20060118X.
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 and increased risk of infection during procedures.
The suture is non-sterile, meaning it may not meet surgical cleanliness standards. This could increase the risk of infection at the surgical site and compromise the sterile field during procedures.
Surgical professionals and patients using the recalled suture for soft tissue approximation. Those with the product number CV2293 and lot 20060118X are most at risk.
Check for product number CV2293 and lot number 20060118X on the suture packaging. The suture is labeled as 'Velosorb 5/0 Undyed 30" KV-11, TaperCutting'.
Look for product number CV2293 and lot number 20060118X on the suture packaging.
The recall states the suture is non-sterile, which could increase infection risk during surgery. It is not recommended for use.
The recall does not specify a remedy, so check the product details and contact the manufacturer if you have concerns.
The suture is indicated for soft tissue approximation of skin and mucosa where 7-10 days of wound support is needed, but not for ligation or specialized procedures.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0031-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0031-2021 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.
