Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0075-2023 — Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only; b) 19262T, OUS only; c) 19272T, OUS only; Microbial medical gas filter, single-use,

U.S. FDA — Device Enforcement · United States · 2022-08-29 · Class I

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0075-2023
Date of alert
2022-08-29
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
TELEFLEX LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04026704400492
Reported risk: Incidents of device splitting or detaching during use
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.