Ornithine Decaboxylase Tablets (2019-06-20)

Starting date:

June 20, 2019

Posting date:

March 6, 2020

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-72481

Last updated: 2020-03-10

• Reason
• Affected products

Affected Products

Ornithine Decaboxylase Tablets

Reason

A recall notification was received on June 19, 2019 from the manufacturer, Rosco Diagnostics A/S, regarding a confirmed loss of activity in a small fraction of the ornithine decaboxylase tablets, lot #1801-1.

Affected products