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

Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588 keV. — recall Z-1296-2015

U.S. FDA — Device Enforcement · United States · 2012-04-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1296-2015
Date of alert
2012-04-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10275879
Reported risk: Radial motor drives replaced during a customer service action were incorrectly assembled backwards.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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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.