Riverpoint Medical recalls non-sterile Velosorb 2/0 absorbable suture (Product CV417G) due to infection risk in surgeries. Affected units may cause surgical site infections if used without proper sterility.
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 non-sterile Velosorb surgical sutures that could lead to infections if used in procedures. This affects surgeons and medical staff who might use the suture without proper sterilization.
The suture is non-sterile, meaning it can't be used in a sterile surgical field. If used without proper sterilization, it could lead to surgical site infections and increase the risk of complications.
Surgeons and medical staff who use the recalled Velosorb suture for soft tissue repairs are most at risk. Patients undergoing surgery with this suture could face infection if the suture isn't properly sterilized.
Check for Product Number CV417G on the suture packaging. The suture is labeled as 'Velosorb 2/0 Undyed 30" V-20 Taper' and was sold with Lot Number 20051406X.
Verify if the suture is sterile by checking for a sterile packaging label or contact the manufacturer for confirmation.
No, the suture is non-sterile and should not be used in surgical procedures without proper sterilization.
Contact Riverpoint Medical directly to confirm if your suture is affected and check for proper sterilization.
Only if it's properly sterilized; otherwise, it could cause surgical site infections.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0015-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0015-2021 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.
