Rebilda Post (2021-01-13)

Starting date:

January 13, 2021

Posting date:

January 22, 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-74835

Last updated:
2021-01-22

• 
  Reason
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  Affected products

Affected Products 

Rebilda Post

Reason

Due to an error in the modification of the product equipment, the following items were inadvertently assembled and partially marketed without parts of the instructions for use.

Affected products