TELEFLEX LLC: Medical Device Recall in 2022 - (Recall #: Z-0077-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Filter + Catheter Mount, REF 191667-000100, OUS only. Catheter mount for circuit-patient connection (Endotracheal tube and mask)

Product Classification:

Class I

Date Initiated: August 29, 2022

Date Posted: October 26, 2022

Recall Number: Z-0077-2023

Event ID: 90816

Reason for Recall:

Incidents of device splitting or detaching during use

Status: Ongoing

Product Quantity: 12 units

Code Information:

UDI: (01)04026704561544(17)250728(10)KMH20H0092, (01)04026704561544(17)250728(10)KMH20H0109, (01)04026704561544(17)251028(10)KMH20L0312, (01)04026704561544(17)251028(10)KMH20L0344, (01)04026704561544(17)251128(10)KMH20M0237, (01)04026704561544(17)251228(10)KMH21A0033, (01)04026704561544(17)260128(10)KMH21B0197, (01)04026704561544(17)260328(10)KMH21D0181, (01)04026704561544(17)260828(10)KMH21J0103, (01)04026704561544(17)260828(10)KMH21J0150, (01)04026704561544(17)261228(10)KMH22A0181, (01)04026704561544(17)261228(10)KMH22A0185.

Distribution Pattern:

US nationwide distribution

Voluntary or Mandated:

Voluntary: Firm initiated