Riverpoint Medical recalls Velosorb 4/0 undyed suture due to non-sterile condition, which could cause surgical site infections. Affected units have Product Number SV496 and Lot Number 20060116FX.
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 compromise the sterile field during procedures.
The suture is non-sterile, meaning it lacks the required cleanliness for surgical use. This increases the chance of infection at the surgical site and may weaken the suture's ability to hold together over time.
Surgical professionals and patients who use this specific suture product for soft tissue approximation. Those with the Product Number SV496 and Lot Number 20060116FX are most at risk.
Check for Product Number SV496 and Lot Number 20060116FX on the suture packaging. This product was sold for soft tissue approximation procedures requiring 7-10 days of wound support.
Look for Product Number SV496 and Lot Number 20060116FX on the suture packaging.
No, this suture is non-sterile and intended only for soft tissue approximation procedures requiring 7-10 days of wound support. It is not for use in ligation, ophthalmic, cardiovascular, or neurological procedures.
The recall record does not specify a remedy, so check the product details and contact the manufacturer if you have concerns.
The recall indicates it is non-sterile, so it should not be used for surgical procedures to avoid infection risks.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0029-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0029-2021 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.
