FDA Device recall Z-2761-2016
Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon
- FDA Device
- Class II
- terminated
- Published 2016-09-14
On 2016-09-14 the FDA classified a Class II recall of Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon by Riverpoint Medical, citing nylon Surgical Sutures are recalled because the seals may become open during distribution or subsequent packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2761-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-08-05 |
| Published | 2016-09-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Riverpoint Medical |
| Distribution | US |
Product
Nylon Surgical Suture for human use and vet use, sold under brand name Riverlon, Securolon, Weblon. Product is sterile. Part numbers: 663BK 663BL 664BL 928BK Product Usage: For use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic, and neurological surgery.
Reason
Nylon Surgical Sutures are recalled because the seals may become open during distribution or subsequent packaging.
Identifiers
| code_info | Lot For human use: 160210-02. Lots For Vet use: 160223-03V 160302-06V 160202-01V 160217-02V 160224-03V 160218-03V 160204-01 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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All Riverpoint Medical recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2761-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.