TELEFLEX LLC: Medical Device Recall in 2022 - (Recall #: Z-0073-2023)

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:

Iso-Gard Filter S, with Expandi-Flex, REF: a) 19261, OUS only; b) 19272, OUS only; Microbial medical gas filter, single-use

Product Classification:

Class I

Date Initiated: August 29, 2022

Date Posted: October 26, 2022

Recall Number: Z-0073-2023

Event ID: 90816

Reason for Recall:

Incidents of device splitting or detaching during use

Status: Ongoing

Product Quantity: 7 units

Code Information:

a) 19261, UDI: (01)04026704388486(17)260128(10)KMH21B0193, (01)04026704388486(17)251028(10)KMH20L0234, (01)04026704388486(17)260828(10)KMH21J0246, (01)04026704388486(17)261028(10)KMH21L0294, (01)04026704388486(17)261228(10)KMH22A0230; b) 19272, UDI: (01)04026704388509(17)260428(10)KMZ21E0613, (01)04026704388509(17)260528(10)KMZ21F0939

Distribution Pattern:

US nationwide distribution

Voluntary or Mandated:

Voluntary: Firm initiated