Riverpoint Medical recalls Velosorb 4/0 absorbable suture due to non-sterile condition, which could cause surgical site infections. Affected units have UDI 20884521151731.
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 sutures because they are non-sterile. This increases the risk of surgical site infections and could compromise the sterile field during surgery.
The suture is non-sterile, meaning it lacks the required cleanliness for surgical use. This can lead to infections at the surgical site and reduce the suture's ability to hold together properly during healing.
Surgical professionals and patients who have received this specific suture product are affected. Those performing procedures requiring sterile field maintenance are at higher risk.
Check for the product name 'Velosorb 4/0 Undyed 30" P-12 Cutting SV426' with UDI number 20884521151731. This suture was sold with lot number 20060813FX.
Verify the product name and UDI number to confirm if you have the recalled suture.
No, this suture is non-sterile and intended only for specific surgical procedures where sterile field maintenance is critical.
The recall record does not specify a remedy, so check with your healthcare provider or the manufacturer for guidance.
The product is indicated for soft tissue approximation of skin and mucosa, but not for ligation, ophthalmic, cardiovascular, or neurological procedures.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0040-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0040-2021 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.
