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

Recall Z-1556-2022 — Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only

U.S. FDA — Device Enforcement · United States · 2022-06-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1556-2022
Date of alert
2022-06-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Micro Therapeutics, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
847536006270
Reported risk: Outer carton packaging of microcatheters were exposed to wet substance during transport.
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.

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