Riverpoint Medical recalls Velosorb 4/0 undyed 30" suture (product SV2294) due to non-sterile condition, which may cause surgical site infections. Affected units sold with UDI 20884521151403.
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 (product SV2294) because it's non-sterile. This could lead to surgical site infections during procedures, especially if used in wound care where sterility is critical.
The suture is non-sterile, meaning it lacks the required cleanliness to prevent infection during surgery. This increases the chance of surgical site infections, particularly in procedures requiring only 7-10 days of wound support.
Surgical professionals and patients who have received this specific suture product for wound care. Those using it for skin or mucosal repairs are most at risk of infection.
Check for product number SV2294 and UDI 20884521151403 on the packaging. This suture is sold for soft tissue repairs where 7-10 days of wound support is needed.
Look for product number SV2294 and UDI 20884521151403 on the packaging to confirm if you have the recalled item.
No, this suture is non-sterile and intended only for specific soft tissue repairs where 7-10 days of wound support is needed. It is not for ligation, ophthalmic, cardiovascular, or neurological procedures.
The recall does not specify a remedy, so check the product details to confirm if you have the recalled item. If you do, contact the manufacturer for guidance.
The recall states it may increase risk of surgical site infections, but does not mention serious injury mechanisms like cuts or fires. The hazard is low risk for most users.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0014-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0014-2021 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.
