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

Recall Z-1481-2013 — BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView SPECT is a gamma camera designed for single or dual detector nuclear imaging accommodating a broad range of emission computed tomography Emission Computed Tomography (ECT) studi

U.S. FDA — Device Enforcement · United States · 2013-04-25 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1481-2013
Date of alert: 2013-04-25
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): 40000092

Reported risk: Philips has received one report from the field that there was an unexpected motion of the detector due to a failure of the mechanical assembly.

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.

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