U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
On 9/1/2010 bomimed, inc. winnipeg, mb, canada initiated a recall of their bomimed integrated reusable laryngoscope blades (macintosh & miller styles - all sizes), model #ol-32d0 to ol-32d4 & ol-32e00, ol-32e0, ol-32e1, ol-32e2, ol-32e3, ol-32e4.
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BOMImed sent a "Medical Device Safety Alert & Correction Action" letter by Fax and Mail on 11/25/2010 to the consignee. The product issue was described and recommended actions to mitigate risk were provided. Contact number is 1-800-667-6276 ext. 234.