TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1931-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380055

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1931-2023

Event ID: 92373

Reason for Recall:

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

Status: Ongoing

Product Quantity: 1670 units

Code Information:

UDI/DI 14026704340672, Batch Numbers: 19ET11, 19GT51, 19JT20, 20AT13, KME20H2315, KME21A2778, KME22A0155, KME22A2335, KME22E0288, KME22E1272, KME22F1551

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated