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.
데이터 추가 비고
Microsurgical Knife - Product Code HNN
원인
This voluntary recall has been initiated due to the product puncturing the packing
during rough handling. once the packaging is damaged, the product is no longer
sterile as labeled.
조치
Notification of the recall sent to distributors and users. The 06/08/07 letter requests customers to notify down to the user level. Included in the
Recall Notification Letter are instructions: "In addition, if you may have further distributed this product, please identify your customers and notify them at once ofthis product recall. Your notification to your customers may be enhanced by including a copy of this recall notification letter. This recall should be carried out to the user level. Your assistance is appreciated and necessary to prevent any inconvenience."