FDA Medical Device Recalls (openFDA)
Teleflex Medical: 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.
- Recall number
- Z-0826-2015
- Recalling firm
- Teleflex Medical
- 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.
- Status
- Terminated
- Initiated
- 2014-12-03
- Posted
- 2014-12-17
- Terminated
- 2017-11-24
- Reason
- The manufacturing dates and expiration dates were transposed on the Tyvek label.
- Root cause
- Labeling Change Control
- Action
- Consignees were notified by letter on 12/03/2014.
- Quantity
- 3180 units
- Distribution
- US (nationwide) including the states of AL, CA, FL, DE, IA, IL, IN, KY, MA, MN, NC, NE, NJ, NY, NV, OH, OK, PA, TX, VA, VT, and WA.
- Lot, serial or model codes
- Product Code: 523300, Lot number: 01B1400034
- 510(k) numbers
- ["K800079"]
- PMA numbers
- not on file
- Product code
- FZP
- Firm FEI
- 3005747797
- Firm city
- Durham
- Firm state
- NC
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28