Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which could lead to surgical site infections. Affected units have UDI 1088452:1149595.
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 3/0 absorbable sutures because they are non-sterile. This could lead to surgical site infections during procedures and increase the risk of complications.
The suture is non-sterile, meaning it lacks the required cleanliness for surgical use. This can compromise the sterile field during procedures, potentially leading to infections at the surgical site. The risk is increased if the suture is used without proper sterilization.
Surgical professionals and patients who have received this specific suture product. Those performing procedures requiring sterile field maintenance are most at risk.
Check for the product name 'Velosorb 3/0 Undyed 30" PC-11 SV487G' with UDI 10884521149595. This suture was sold with lot number 20060814X.
Identify the product by checking the UDI number 10884521149595 and lot number 20060814X.
No, this suture is non-sterile and could lead to surgical site infections if used without proper sterilization.
Check the UDI number and lot number to confirm if you have the recalled product. The recall does not specify a remedy.
The recall states the suture is non-sterile, so it should not be used for surgical procedures without proper sterilization.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0041-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0041-2021 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.
