Teleflex Medical: Medical Device Recall in 2018 - (Recall #: Z-0705-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.

Product Classification:

Class II

Date Initiated: January 10, 2017

Date Posted: March 7, 2018

Recall Number: Z-0705-2018

Event ID: 78929

Reason for Recall:

The pouch may contain the incorrect Rusch Green Lite product size. Pouches that are labeled as containing RUSCH GREEN LITE MAC 1 may instead contain RUSCH GREEN LITE MAC 2.

Status: Terminated

Product Quantity: 2140 units

Code Information:

Lot/Serial number: 1602312

Distribution Pattern:

US only

Voluntary or Mandated:

Voluntary: Firm initiated