Medline Industries Inc: Medical Device Recall in 2017 - (Recall #: Z-0112-2018)

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:

MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER, 8Fr, REF DYNCPE8

Product Classification:

Class II

Date Initiated: October 10, 2017

Date Posted: November 29, 2017

Recall Number: Z-0112-2018

Event ID: 78319

Reason for Recall:

Products labeled as sterile were distributed prior to sterilization

Status: Terminated

Product Quantity: 190 units

Code Information:

Lot 2861707008

Distribution Pattern:

FL, IN, TN, GA, NJ, UT, MD, Nicaragua, Honduras

Voluntary or Mandated:

Voluntary: Firm initiated