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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Ge healthcare has become aware of a potential safety issue where certain power cords could overheat. the affected power cords were manufactured by electri-cord and are referred to as "taller bridge" power cords. the overheating of the power cord could result in fire charring smoke or sparking where the power cord connects to the wall outlet which could cause thermal injury. there have been no injuries reported as a result of this issue.
Model Catalog: N/A - EXAM LIGHT ONLY (Lot serial: ALL); Model Catalog: 3400 (Lot serial: ALL); Model Catalog: 6600-0427-900 (Lot serial: ALL); Model Catalog: 3500 (Lot serial: ALL); Model Catalog: 4400 (Lot serial: ALL); Model Catalog: 3300 (Lot serial: ALL); Model Catalog: 6600-0845-800 (Lot serial: ALL); Model Catalog: 4000 ACCESS (Lot serial: ALL); Model Catalog: OMNIBED (Lot serial: ALL); Model Catalog: 120 VOLT (Lot serial: ALL)
제품 설명
GIRAFFE EXAM LIGHT;INFANT WARMER SYSTEM;Ohmeda Medical Panda Baby Warmer;Giraffe Spot PT Lite Phototherapy System;Care Plus Incubator;GIRAFFE OMNIBED;GIRAFFE INCUBATOR