Remel Fluid Thio Med (10ml) (2019-03-20)

Starting date:

March 20, 2019

Posting date:

April 5, 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-69496

Last updated: 2019-04-05

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  Reason
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  Affected products

Affected Products

Remel Fluid Thio Med (10ml)

Reason

This product may fail performance testing starting at 141 days after date of manufacture (Aug 15, 2018).

Affected products