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

Recall Z-0113-2016 — MAJ-1606 Instrument Channel Adaptor; a single use adapter which enables a connection between the endoscope's instrument channel port and the O FP-2 pump's tubing.

U.S. FDA — Device Enforcement · United States · 2015-09-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0113-2016
Date of alert
2015-09-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Olympus Corporation of the Americas
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
20115441
Reported risk: small puncture marks in a sterile package for an accessory to an Olympus device
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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