Teleflex Medical: Medical Device Recall in 2017 - (Recall #: Z-2130-2017)

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:

INFANT 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-2130-2017

Event ID: 77081

Reason for Recall:

Status: Terminated

Product Quantity: 19,043 units in total

Code Information:

Product Code: PE103, Lot numbers: 02B1300991, 02B1402029, 02C1301654, 02E1201155, 02H1302224, 02K1100520, 02K1103125, 02K1200732, 02K1202185, 02L0701465, 02L0701959, 02L1201668, 02L1203112, 02M1201149, 74A1601005 & 74F1400876.74H1601152, 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