Riverpoint Recalls Non-Sterile Velosorb Fast Braided Absorbable Sutures
Riverpoint Medical is recalling 1,248 units of non-sterile Velosorb sutures due to a risk of surgical site infection.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk of surgical site infection, which is a significant health hazard, but the source text does not report any specific illnesses or injuries, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.
Plain-English summary
Riverpoint Medical, LLC is recalling 1,248 units of Velosorb Fast Braided Absorbable Sutures (Product Number: CV1213, Lot Number: 20052817X). The affected products were distributed nationwide in the United States.
The recall was initiated because the surgical sutures are non-sterile. The use of these non-sterile sutures could compromise the sterile field, increase the risk of a surgical site infection, and increase break strength retention.
Healthcare facilities and consumers should stop using the affected sutures immediately and contact Riverpoint Medical for further instructions.
The recalled product
- Product
- Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 5/0 Undyed 30" CV-23 Taper, Product Number: CV1213, UDI: 20884521150758 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not
- Manufacturer
- Riverpoint Medical, LLC
- Hazard
- Affected units
- 1,248
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot Number: 20052817X
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 40 recalled by Riverpoint Medical, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 40 products in this recall →Related recalls
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