Riverpoint Medical recalls non-sterile Velosorb 3/0 absorbable suture (Product CV416G) due to infection risk. This suture may cause surgical site infections if not sterile.
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 non-sterile Velosorb surgical sutures that could lead to infections during surgery. Using these sutures without proper sterility could increase infection risks for patients.
The suture is non-sterile, meaning it lacks the required cleanliness for surgical procedures. This can compromise the sterile field during surgery, increasing the chance of surgical site infections. The suture is designed for short-term wound support (7-10 days) but not for critical procedures.
Surgical teams and hospitals using the recalled Velosorb 3/0 suture (Product Number CV416G) are affected. Patients undergoing surgery with this suture may face higher infection risks.
Check for Product Number CV416G on the suture packaging. The suture is labeled as 'Covidien Velosorb 3/0 Undyed 30" V-20 Taper' and was sold with Lot Number 20052815X.
Verify if the suture is sterile by checking the packaging for a sterile label or contact the manufacturer for confirmation.
No, this suture is intended only for soft tissue approximation of skin and mucosa where 7-10 days of wound support is needed. It is not for use in ligation, ophthalmic, cardiovascular, or neurological procedures.
Look for Product Number CV416G on the suture packaging. The suture is labeled as 'Covidien Velosorb 3/0 Undyed 30" V-20 Taper' and was sold with Lot Number 20052815X.
The recall does not specify a remedy, so contact Riverpoint Medical directly for guidance on handling the suture.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0026-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0026-2021 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.
