Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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원인
Siemens healthcare diagnostics has identified a potential pinch hazard in the interior of clinitek novus analyzer. the potential pinch hazard is in the area of the syringe pump and is only present when the instrument is operating with the front cover open. the instrument can operate with the front cover open during the "systems sequence test" mode for troubleshooting and/or maintenance.
Model Catalog: 10494134 (Lot serial: ALL LOTS); Model Catalog: 10844545 (Lot serial: ALL LOTS); Model Catalog: 10697937 (Lot serial: ALL LOTS); Model Catalog: 10844557 (Lot serial: ALL LOTS)
제품 설명
CLINITEK NOVUS AUTOMATED URINE CHEMISTRY ANALYZER (WITH RACK HANDLER)