Teleflex Medical: Medical Device Recall in 2019 - (Recall #: Z-2086-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Rusch EasyCath Kit

Product Classification:

Class II

Date Initiated: July 1, 2019

Date Posted: August 7, 2019

Recall Number: Z-2086-2019

Event ID: 83250

Reason for Recall:

Potential for product not to be sterile.

Status: Terminated

Product Quantity: 3,700 devices

Code Information:

Catalog Number ECK120, Lot Number 74C1900304, Expiration Date 03/01/2022. Catalog Number ECK125, Lot Number 74B1901676, Expiration Date 06/01/2022.

Distribution Pattern:

Nationwide distribution to CA, FL, IL, NC, NJ, OH, OK, TX.

Voluntary or Mandated:

Voluntary: Firm initiated