Teleflex Medical: Medical Device Recall in 2014 - (Recall #: Z-1534-2014)

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:

CAPIO, Monodeck, Violet Monofilament Polydioxanone Suture, 1 x 48 inches (122cm) Absorbable Surgical Suture, Rx Only, Teleflex Medical. Product Code: 833-137.

Product Classification:

Class II

Date Initiated: March 11, 2014

Date Posted: May 7, 2014

Recall Number: Z-1534-2014

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: 833-137, Lot numbers: 02A0901938, 02B0901537, 02H1001025, 02H1001026, 02H1001027, 02C1102979, 02C1102983, 02D1300294, 02D1301164, 02C1302078, 02D1302468.

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