Riverpoint Medical recalls Velosorb 4/0 undyed 30" absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have Product Number SVP2294 and Lot Number 20052017FX.
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 compromise the sterile field during procedures.
The suture is non-sterile, meaning it lacks the required cleanliness for surgical procedures. This increases the risk of infection at the surgical site and may weaken the suture's ability to hold tissue together over time.
Surgical professionals and patients who received this specific suture product are affected. The risk is low for most users as it's a non-sterile product used in short-term wound support.
Check for Product Number SVP2294 and Lot Number 20052017FX on the packaging. This suture is used for short-term wound support in soft tissue, not for ligation or sensitive procedures.
Look for Product Number SVP2294 and Lot Number 20052017FX on the packaging to confirm if the item is affected.
No, this suture is non-sterile and intended only for short-term wound support in soft tissue. It is not for use in ligation or sensitive procedures.
The recall does not specify a remedy, so check the product details to confirm if it's affected and contact the manufacturer for further guidance.
The recall states it may increase the risk of infection but does not mention serious injury mechanisms. The hazard level is low risk.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0019-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0019-2021 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.
