FDA Device recall Z-0826-2015
WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips
- FDA Device
- Class II
- terminated
- Published 2014-12-24
On 2014-12-24 the FDA classified a Class II recall of WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips by Teleflex Medical, citing the manufacturing dates and expiration dates were transposed on the Tyvek label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0826-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-12-03 |
| Published | 2014-12-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Teleflex Medical |
| Distribution | US |
Product
WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended for use in procedures involving vessels or anatomic structures for which the surgeon determines ligating clips are the best choice.
Reason
The manufacturing dates and expiration dates were transposed on the Tyvek label.
Identifiers
| code_info | Product Code: 523300, Lot number: 01B1400034 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0826-2015%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.