Teleflex Medical: Medical Device Recall in 2014 - (Recall #: Z-1535-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Dekna-lok, 1 x 17.78 cm, Violet Braided Polyglycolic Acid Coated Suture, Synthetic Absorbable Surgical Suture USP, Rx Only, Sterile. Teleflex Product Code: 200101-01.

Product Classification:

Class II

Date Initiated: March 11, 2014

Date Posted: May 7, 2014

Recall Number: Z-1535-2014

Event ID: 67973

Reason for Recall:

The product did not meet minimum and/or average minimum Teleflex resorption strength requirements.

Status: Terminated

Product Quantity: 7,380 ea (total)

Code Information:

Product Code: 200101-01, Lot # 02F0801290 and Product Code: BP1000V2L, Lot numbers: 02C1003535 & 02F1000711.

Distribution Pattern:

Worldwide Distribution - US Nationwide in the states of CA, CO, GA, LA, IL, MA, MI, MN, MO, NC, and in the countries of Ireland and Singapore.

Voluntary or Mandated:

Voluntary: Firm initiated