Riverpoint Medical recalls non-sterile Velosorb 3/0 absorbable suture (product CV3110) due to infection risk. Use may compromise sterile field and cause surgical site infections.
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 during surgery. This affects patients and surgeons using the product for skin and mucosal repairs.
The suture is non-sterile, meaning it doesn't meet surgical cleanliness standards. Using it during procedures could introduce infections and increase the chance of surgical site infections.
Patients and surgeons who use this suture for skin and mucosal repairs. Those using it for procedures requiring sterile field maintenance are most at risk.
Check for product number CV3110 on the suture packaging. The suture is labeled as 'Covidien Velosorb 3/0 Undyed 30" CV-25 Taper' for soft tissue repairs.
Look for product number CV3110 on the suture packaging to confirm if it's recalled.
No, this suture is not intended for use in ligation, ophthalmic, cardiovascular, or neurological procedures. It's only for soft tissue repairs where 7-10 days of wound support is needed.
The recall record does not specify a remedy, so check the product packaging for the product number CV3110 to confirm if it's affected.
The recall states it's non-sterile and could increase infection risk, but it does not mention a risk of serious injury or death.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0018-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0018-2021 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.
