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

Recall Z-0450-2015 — BrightView product code: 882478 BrightView X product code: 882480 BrightView XCT product code: 882482 and 882454

U.S. FDA — Device Enforcement · United States · 2014-11-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0450-2015
Date of alert: 2014-11-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Philips Medical Systems (Cleveland) Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 11000022

Reported risk: Software issues

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.

Recall Z-0450-2015 — BrightView product code: 882478 BrightView X product code: 882480 BrightView XCT product code: 882482 and 882454

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