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Bard marquee disposable core biopsy instrument kit
Official notice
21 Aug 2023
Last checked
21 Aug 2023
An official Health Canada notice concerns Bard marquee disposable core biopsy instrument kit. BD has received complaints regarding mismatch between the coaxial and the needle in Bard® Marquee® kit devices, where the coaxial cannula inner diameter prohibits the biopsy needle from properly fitting into the coaxial cannula and accessing the target tissue. Recall Start Date: August 10, 2023 Published 2023-08-21.
What to do now
Review notice & share with users, discontinue/dispose affected inventory, complete/return reply form.
Recall number
74142
Official notice
2023-08-21
The hazard
The hazard
BD has received complaints regarding mismatch between the coaxial and the needle in Bard® Marquee® kit devices, where the coaxial cannula inner diameter prohibits the biopsy needle from properly fitting into the coaxial cannula and accessing the target tissue. Recall Start Date: August 10, 2023
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Manufacturer
Phone
Brand: Bard Peripheral Vascular, Bard Marquee Disposable Core Biopsy Instrument Kit.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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