TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-1962-2023)

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 Magill, High Volume, Low Pressure Cuff, REF 112080075

Product Classification:

Class I

Date Initiated: May 25, 2023

Date Posted: July 5, 2023

Recall Number: Z-1962-2023

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: 13810 units

Code Information:

UDI/DI Batch Numbers: 18FT26, 18GG17, 18GG19, 18HG15, 18HG37, 18IG04, 18IG29, 18JG17, 18KG10, 19AT23, 19CT64, 19ET12, 19ET24, 19GT31, 19HT69, 19IT11, 20AT22, 20BT13, 20BT42, 20CT02, 20CT54, 20DT09, 20FT21, 20FT60, 20GT18, KME20H0334, KME21F1534, KME22A2269, KME22B0741, KME22B0896, KME22B1031, KME22C0096, KME22E2348, KME22F2118,

Distribution Pattern:

US Nationwide distribution including Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated