RecallDepth

WECK Horizon" Manual-Load Ligating Clip Applier, For Medium-Large Size Horizon Ligation Clips Curved Jaw, 11 (28cm), Rx Only, REF 337111, Product Usage: Weck Closure Systems applier has been designed and calibrated for use with specific Horizon, Hemoclip Plus Hemoclip Traditional, or Atrauclip ligating clips as indicated. Applier color coding matches the color of the ligating clip cartridge for which it is to be used. Hemoclip Plus appliers are easily identified by one black-ring handle.

This recall has been terminated (originally issued September 8, 2016).

Company
Teleflex Medical
Recall Initiated
August 24, 2016
Posted
September 8, 2016
Terminated
August 25, 2017
Recall Number
Z-2759-2016
Quantity
49 units
Firm Location
Research Triangle Park, NC
Official Source
View on FDA website ↗

Reason for Recall

Misbranded: Incorrect etching on the device.

Distribution

Worldwide Distribution US Nationwide in the states of FL, IL, KY, MI, NY and OK and countries of Mexico and Canada.

Lot / Code Info

Product Code: 337111, Lot Number: 06F1515745.

Root Cause

Error in labeling

Action Taken

Teleflex sent an Urgent Medical Device Notification letter dated August 24, 2016 to customers via FedEx. The letter identified the affected product, problem and actions to be taken. For questionscontact your local sales representative or Customer Service at 1-866-246-6990.

More recalls by Teleflex Medical

View all recalls by this company →