WECK Hemoclip Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended for use in procedures involvi
FDA device recall Z-0826-2015 · posted 2014-12-17 · Terminated
Recall details
- Recalling firm
- Teleflex Medical
- Reason for recall
- The manufacturing dates and expiration dates were transposed on the Tyvek label.
- Action taken
- Consignees were notified by letter on 12/03/2014.
- Root cause
- Labeling Change Control
- Status
- Terminated
- Product code
- FZP
- Quantity affected
- 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.
- Date initiated
- 2014-12-03
- Date posted
- 2014-12-17
- Date terminated
- 2017-11-24
- Location
- Durham, NC
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| HEMOCLIP SURGICAL OCCLUDING CLIP (K800079) | Edward Weck, Inc. | 1980-01-28 |