Riverpoint Medical recalls Velosorb 3/0 absorbable sutures due to non-sterile condition, which may increase surgical site infections. Affected products include specific lot numbers and product codes.
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 could lead to surgical site infections or increased risk of infection during procedures.
The suture is non-sterile, meaning it does not meet surgical cleanliness standards. This can compromise the sterile field during procedures, potentially increasing the risk of infection at the surgical site. The suture may also retain break strength longer than intended, which could affect wound healing.
Surgical professionals and patients who have purchased the specific Velosorb 3/0 undyed 18" P-14 cutting suture with product number SV6830. Those using the product for soft tissue approximation are most at risk.
Check for product number SV6830 on the packaging. The suture is undyed, 3/0 size, 18 inches long, and labeled as P-14 cutting. It was sold with lot number 20051814FX.
Verify the product number SV6830 and lot number 20051814FX on the packaging.
No, the suture is non-sterile and intended only for soft tissue approximation where 7-10 days of wound support is needed. It is not for use in ligation, ophthalmic, cardiovascular, or neurological procedures.
The recall does not specify a remedy, so check the product details and contact the manufacturer if you have concerns.
The recall states it may increase risk of surgical site infections but does not mention serious injury mechanisms like cuts or fires.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0016-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0016-2021 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.
