Riverpoint Medical recalls Velos: non-sterile surgical suture that could cause infections during procedures. Affected units have specific product numbers and lot dates.
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 due to being non-sterile. This increases infection risk during surgery and may weaken the suture's ability to hold wounds together.
The suture is non-sterile, meaning it can introduce bacteria during surgery. This could lead to infections at the surgical site. The suture may also break more easily than intended, affecting wound healing.
Surgical patients and healthcare providers who use the recalled suture for soft tissue repairs. Those with the specific product number and lot date are most at risk.
Check for product number CV605 and lot number 20060201X on the packaging. The suture is labeled as 'Covidien Velosorb 1 Undyed 36" GS-25' for soft tissue repairs.
Look for product number CV605 and lot number 20060201X on the packaging.
No, the recall specifies it is only for soft tissue repairs where 7-10 days of wound support is needed, not for ligation, ophthalmic, cardiovascular, or neurological procedures.
The recall does not specify a remedy, so check with your healthcare provider for guidance on safe alternatives.
The recall states it may increase infection risk and break strength retention, but does not mention life-threatening hazards.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0034-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0034-2021 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.
