CanadaThe Brevera® Breast Biopsy System (model/catalogue number BREVDISP09) manufactured by Hologic, Inc. is affected. The device is being removed because metal and plastic particles may be dislodged from the device during use. Quarantine any units in your inventory, do not use them, and return the product to Hologic.
What's being recalled
Companies: Hologic, Inc., 250 Campus Drive, Marlborough, Massachusetts, United States, 01752.
How to identify it
Affected products: Brevera® Breast Biopsy System; Affected products: Not applicable.; Model or catalogue number: BREVDISP09
The hazard
The subject device is being removed because there is a risk of metal and plastic particles being dislodged from the device during use.
What to do
Quarantine any subject product units you currently have in your inventory and return the subject product to Hologic. Do not use the subject product.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)
United States