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

Recall Z-1746-2014 — IntelliVue MX40 Wearable Patient Monitor in use with the Philips IntelliVue Information Center iX (PIIC iX); 865350, 865351, 865352

U.S. FDA — Device Enforcement · United States · 2014-05-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1746-2014
Date of alert
2014-05-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips Medical Systems, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00700001
Reported risk: IntelliVue MX40 (part numbers 865350, 865352) with software revisions B.00 or B.01 may not resume alarming when the alarms are paused and the pause timer ends.
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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