Recall Z-1293-2014— Teleflex Medical

Name: FDA recall Z-1293-2014
Creator: U.S. Food and Drug Administration
Published: 2014-03-11

Class II · Terminated

Class II FDA medical device recall by Teleflex Medical, initiated 2014-03-11, terminated 2017-08-15. It names one FDA 510(k) clearance: K021019. Product: Sutures, Non-absorbable, Synthetic, Polypropylene, Sterile, Rx only, Product Usage: Non-absorbable polypropylene surgical suture is a monofilament, Non-absorbable, sterile, flexible thread prepared from long-chain polyolefin polymer known as polypropylene and is indicated for use in soft tissue approximation.. Reason: The products are being recalled because they did not meet minimum needle attachment strength requirements..

Recalling firm: Teleflex Medical
Classification: Class II
Status: Terminated
Initiated: 2014-03-11
Terminated: 2017-08-15
Firm location: Research Triangle Park, NC, United States

510(k) clearances named in this recall

1 on FDA's record

K021019 — COTTONY II, SILKY II POLYDEK & TEVDEK II POLYESTER SUTUREGenzyme Corp.·cleared 2002-06-18

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Sutures, Non-absorbable, Synthetic, Polypropylene, Sterile, Rx only, Product Usage: Non-absorbable polypropylene surgical suture is a monofilament, Non-absorbable, sterile, flexible thread prepared from long-chain polyolefin polymer known as polypropylene and is indicated for use in soft tissue approximation.

Reason for recall

The products are being recalled because they did not meet minimum needle attachment strength requirements.

Data sourced from openFDA. This site is unofficial and independent of the FDA.