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Terminated

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.

FDA Recall Z-0826-2015 · Posted 2014-12-17

Recalling FirmTeleflex Medical
Recall StatusTerminated
Product CodeFZP
Date Initiated2014-12-03
Date Terminated2017-11-24
Product Quantity3180 units

Reason for Recall

The manufacturing dates and expiration dates were transposed on the Tyvek label.

Firm Action

Consignees were notified by letter on 12/03/2014.

Root Cause

Labeling Change Control

Distribution Pattern

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.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K800079HEMOCLIP SURGICAL OCCLUDING CLIPEdward Weck, Inc. · 1980-01-28

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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