Riverpoint Medical recalls non-sterile Velosorb 4/0 suture to prevent surgical site infections. The recall affects specific product numbers sold in 2023. Consumers should check labels for product number CV3100.
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 fast braided absorbable sutures to prevent surgical site infections. Using these sutures could increase infection risk during surgery.
The suture is non-sterile, meaning it lacks the required cleanliness for surgical procedures. This could lead to infections at the surgical site if used improperly. The risk is higher when the suture is used in procedures where sterility is critical.
Surgical patients and healthcare providers who used the recalled Velosorb 4/0 suture (product number CV3100) for soft tissue approximation. Those with the specific product number are most at risk.
Check the product label for 'Velosorb 4/0 Undyed 30" CV-25 Taper' and product number CV3100. The recall applies to items sold in 2023 with the UDI code 20884521150901.
Look for the product number CV3100 on the suture packaging or label.
No, the suture is non-sterile and intended only for soft tissue approximation where 7-10 days of wound support is needed. It is not for use in ligation, ophthalmic, cardiovascular, or neurological procedures.
Check the product label for 'Velosorb 4/0 Undyed 30" CV-25 Taper' and product number CV3100. The recall applies to items sold in 2023 with UDI 20884521150901.
The recall does not require immediate action, but you should check the product label to confirm if it is affected. If it is, contact the manufacturer for further guidance.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0024-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0024-2021 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.
