Teleflex Medical: Medical Device Recall in 2017 - (Recall #: Z-2127-2017)

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 STRAIGHT 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-2127-2017

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: PE100, Lot numbers: 02F0801115, 02F0901859, 02G0802748, 02G0900814, 02H0900192, 02K0900567, 02L0900163, 02M0901006, 74A1601695, 74G1500137, 74G1502714 & 74M1400489.

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