D13S319 Plus Deletion Probe (2019-04-24)

Starting date:

April 24, 2019

Posting date:

May 24, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-70015

Last updated: 2019-05-24

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  Reason
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  Affected products

Affected Products

D13S319 Plus Deletion Probe

Reason

This recall has been initiated following a review of the labelling and marketing material for this ASR Probe. We have identified an error with the chromoMap on the package insert which is incorrect.

Affected products