CUSTOM PROCEDURE KIT - STROKE (2021-02-08)

Starting date:

February 8, 2021

Posting date:

August 6, 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, Hospitals, Healthcare Professionals

Identification number:

RA-76159

Last updated:
2021-08-06

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  Reason
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  Affected products

Affected Products 

CUSTOM PROCEDURE KIT - STROKE

Reason

Merit Medical received a Field Safety Notice (FSN) from BD Medical advising of an added caution that intraocular use is not validated by BD for certain syringes and needles.

Affected products