Class II — Riverpoint Medical, LLC
| Recalling firm | Riverpoint Medical LLC |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Polypropylene Surgical Sutures are recalled because the seals may become open during distribution or subsequent packaging. |
| Product | Polypropylene Surgical Sutures, brand Webglo, for vet use. Product is sterile. Part number: GP8665 Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery. |
| Quantity | 61 boxes distributed in the US only |
| Distribution | US Nationwide distribution in the states of ID, MA, OR, NY and in the country of Australia. |
| Initiated | 2016-08-05 |
| Classified | 2016-09-08 |
| Terminated | 2016-12-22 |
| Recall number | Z-2762-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Riverpoint Medical, LLC (Z-2762-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/74891/
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