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

Recall Z-0860-2015 — ADVIA Centaur XP Immunoassay System (including refurbished) Professional use in a laboratory for in vitro diagnostic tests.

U.S. FDA — Device Enforcement · United States · 2014-10-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0860-2015
Date of alert
2014-10-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Healthcare Diagnostics, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10285219
Reported risk: A slight crack of the tubing at the connecting fitting on the reservoir connector assembly may occur due to mechanical stress.
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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