Teleflex Medical: Medical Device Recall in 2017 - (Recall #: Z-2129-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory

Product Classification:

Class II

Date Initiated: April 21, 2017

Date Posted: May 31, 2017

Recall Number: Z-2129-2017

Event ID: 77081

Reason for Recall:

Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.

Status: Terminated

Product Quantity: 19,043 units in total

Code Information:

Product Code: PE102, Lot numbers: 02A1101041, 02B1102552, 02C1001258, 02C1003795, 02C1101253, 02C1104114, 02D0802670, 02D0803968, 02D1000682, 02D1002136, 02D1101334, 02E1001502, 02E1100384, 02F0800281, 02F1000667, 02F1002368, 02F1101766, 02F1102607, 02F1103754, 02G1000322, 02G1001538, 02H0801670, 02H0803375, 02H1000732, 02H1103023, 02H1103940, 02J1000236, 02J1001515, 02J1002609, 02J1003237, 02J1101139, 02J1102143, 02K1000270, 02K1001993, 02K1100519,02K1103124, 02K1301613, 02L0701463, 02L0701958, 02L0702675, 02L1000763, 02M0700783, 02M1001319, 74A1600225, 74A1600226, 74B1601947, 74B1601948, 74D1600917, 74F1401859, 74F1502294, 74F1502573, 74F1602371, 74H1601152, 74J1601641, 74K1501590 & 74L1500555.

Distribution Pattern:

Worldwide Distribution - U.S. Nationwide. Foreign consignees: Australia, Canada, China, Columbia, India, San Salvador, Singapore and South Korea.

Voluntary or Mandated:

Voluntary: Firm initiated