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

Recall Z-0329-2014 — Olympus Endoscopic Flushing Pump, Model OPF-2. Facilitates washing of tissues to remove blood, feces and other organic matter during endoscopic procedures.

U.S. FDA — Device Enforcement · United States · 2013-05-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0329-2014
Date of alert
2013-05-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Olympus America Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
21301567
Reported risk: There is a possibility that the pump head was not shipped in the locked position. If the pump head is in an unlocked position this may, under certain circumstances, cause the pump to stop and go into power stand-by mode.
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.

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.