Riverpoint Medical recalls Velosorb 6/0 absorbable sutures due to non-sterile condition, which may cause 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 6/0 absorbable sutures because they are non-sterile. This could lead to surgical site infections and compromise the sterile field during procedures.
The suture is non-sterile, meaning it lacks the necessary cleanliness to maintain a sterile surgical field. This increases the risk of infection at the surgical site and may weaken the suture's ability to hold tissue together over time.
Surgical professionals and patients who use the recalled Velosorb sutures for soft tissue repairs. Those performing procedures where sterile technique is critical are most at risk.
Check for product number SV4893 and lot number 20052703FX on the packaging. The suture is labeled as 'Covidien Velosorb 6/0 Undyed 30" P-10 Cutting' for soft tissue repairs.
Verify the product number SV4893 and lot number 20052703FX on the packaging to confirm if it is affected.
The recall states the suture is non-sterile, so it is not safe for surgical procedures where sterility is required. It is intended for soft tissue repairs with limited use.
The recall does not specify a remedy, so check the product details to confirm if it is affected and contact Riverpoint Medical for further guidance.
The recall indicates the suture is non-sterile, so it should not be used for surgical procedures to avoid infection risks.
We’ve drafted a message you can send Riverpoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0023-2021 — Riverpoint Medical Riverpoint Medical Hello, I own a Riverpoint Medical that is covered by recall Z-0023-2021 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.
