Teleflex Medical: Medical Device Recall in 2019 - (Recall #: Z-1765-2019)

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:

Sheridan/CF Novaplus 7.0 mm, Product Code V5-10114 Product Usage: Tracheal tube/airway management

Product Classification:

Class I

Date Initiated: May 24, 2019

Date Posted: June 26, 2019

Recall Number: Z-1765-2019

Event ID: 82964

Reason for Recall:

This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the Endotracheal tube.

Status: Terminated

Product Quantity: 77136 units

Code Information:

Lot Numbers: 73K1600156 73K1600735 73L1600501 73A1700120 73B1700321 73C1700425 73D1700630 73E1700504 73G1700146 73H1700053 73J1700307 73K1700085 73B1800223 73B1800371 73C1800372 73D1800655 73E1800579 73G1800627 73H1800203 73H1800429 73H1800758 73J1800118 73J1800696

Distribution Pattern:

Worldwide - US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated