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

eakin Cohesive seal, small, Model Number 839002, ostomy barrier seal — recall Z-3263-2024

U.S. FDA — Device Enforcement · Ireland · 2024-08-08 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3263-2024
Date of alert
2024-08-08
Country / jurisdiction
Ireland
Risk level
Class III
Risk type
recall
Brand
T.G. Eakin Limited
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00768455108732
Reported risk: On lot of cartons of Eakin Cohesive small seals, Model Number 839002 may contain blistered seals labelled as 839005.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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.

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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.