ONCONTROL BONE MARROW BIOPSY SYSTEM (2021-03-08)

Starting date:

March 8, 2021

Posting date:

March 25, 2021

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-75197

Last updated:
2021-05-06

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  Reason
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  Affected products

Affected Products 

ONCONTROL BONE MARROW BIOPSY SYSTEM

Reason

Teleflex is voluntarily recalling the products referenced above due to customers reporting difficulty inserting the biopsy ejector rod into the bone lesion biopsy cannula, preventing the biopsy sample from being collected

Affected products