Teleflex Medical: Medical Device Recall in 2017 - (Recall #: Z-2128-2017)

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 3/8 Y 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-2128-2017

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: PE101, Lot numbers: 02A1100078, 02A1403418, 02B0900484, 02B1201332, 02C1002327, 02C1101252, 02D0802669, 02D0803967, 02D1101333, 02D1101975, 02D1201492, 02E0900909, 02F0800279, 02F1101765, 02G0802046, 02G0900106, 02G0902858, 02G1302277, 02H0901652, 02H0902603, 02H1103939, 02K0900568, 02K1000269, 02K1001997, 02K1103123, 02K1301033, 02L0701464, 02L0901521, 02L1002578, 02L1003527, 74A1601696, 74C1601057, 74E1600942, 74E1602825, 74F1401270, 74H1501378, 74J1502624 & 74L1500554.

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