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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Trays contain sterile lubricant and/or alcohol prep pads manufactured by triad group. on december 22 2010 triad issued a recall notice. the recall is due to concerns expressed by the us fda regarding the validation of the gamma radiation sterilization cycles for these products. a recall was also issued by triad involving alcohol prep pads alcohol swabs and alcohol swabsticks due to concerns about potential contamination with bacillus cereus.
Model Catalog: UT1002 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: UT 8140 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: UT 7030 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: UT 7010 (Lot serial: > 10 lot numbers contact mfg); Model Catalog: UT1002 (Lot serial: >10 CONTACT MFR. OR IMP.); Model Catalog: UT1001 (Lot serial: >10 CONTACT MFR. OR IMP.); Model Catalog: UT 8140 (Lot serial: >10 CONTACT MFR. OR IMP.); Model Catalog: UT 7030 (Lot serial: >10 CONTACT MFR. OR IMP.); Model Catalog: UT 7010 (Lot serial: >10 CONTACT MFR. OR IMP.); Model Catalog: UT1001 (Lot serial: > 10 lot numbers contact mfg)