Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which could increase surgical site infections and break strength retention risks. Affected units include specific product numbers 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 is non-sterile. This could lead to surgical site infections and affect the suture's strength during healing. The recall affects specific product numbers and lot numbers sold for soft tissue repairs.
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 potentially reduce the suture's ability to hold together during healing.
Healthcare professionals using the suture for soft tissue repairs are most at risk. The recall applies to specific product numbers and lot numbers sold between 2006 and 2007.
Check for product number CV916 and lot number 20060120X on the packaging. The suture is sold for soft tissue repairs where only 7-10 days of wound support is needed.
Look for product number CV916 and lot number 20060120X on the packaging.
No, this suture is non-sterile and intended only for soft tissue repairs where 7-10 days of wound support is needed. It is not for use in ligation, ophthalmic, cardiovascular, or neurological procedures.
The recall does not specify a remedy, so check the product details to confirm if it is affected. Contact the manufacturer for further guidance if needed.
The recall states it could increase surgical site infections and break strength retention, but no specific serious injury mechanism is described.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0033-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0033-2021 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.
