RecallDepth

Fixt Suture Bonded Plus Violet Braided Polyglycolic Acid Coated Suture, Synthetic Absorbable Surgical Suture, Sterile, Rx Only, Teleflex Medical. Indicated for use in soft tissue approximation.

This recall has been terminated (originally issued May 7, 2014).

Company
Teleflex Medical
Recall Initiated
March 11, 2014
Posted
May 7, 2014
Terminated
August 14, 2017
Recall Number
Z-1558-2014
Quantity
32,271 ea.
Firm Location
Durham, NC
Official Source
View on FDA website ↗

Reason for Recall

Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.

Distribution

Worldwide Distribution -- USA, including the states of AL, CA, FL, GA, IL, IN, KS, LA, ME, MA, MI, MN, MS, MO, NV, NJ, NM, NY, OH, PA, RI, SC, TN, TX, UT, VA, WV, and WI; and countries of Canada, Germany, and Ireland.

Lot / Code Info

Product Code BON100 - Lot 02H1302839, 02J1101705, 02D1101137, 02F1103013, Product Code EP4049N - Lot 02A1003137

Root Cause

Employee error

Action Taken

Urgent Medical Device Recall Notification letters were issued on March 11, 2014 to consignees. The letter requested that customers discontinue use and quarantine any product on hand. The attached Recall Acknowledgment Form should be completed and returned to Teleflex regardless of whether affected product is on hand or not. Once received a customer service representative will contact customers with instructions on how to return the affected product. Questions should be directed to Customer Service at 1-866-246-6990.

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