Health product recall

M-Eslon Capsule: Product mix-up

Brand(s)
Last updated

Summary

Product
M-Eslon capsule
Issue
Health products - Labelling
What to do

Check your M-Eslon (morphine sulfate) medication bottle or package. If your prescription is for 30 mg capsules and the bottle contains 60 mg capsules, or if you are unsure, do not take these capsules and return them to your pharmacy. If you or someone you are caring for is experiencing an overdose (symptoms are described below), call 911 immediately and seek immediate medical attention

Affected products

Brand Product Name Market Authorization Dosage Form Strength Lot numbers
Ethypharm Inc. M-Eslon 30 mg capsule DIN 02019949 Capsule (Extended release) Morphine sulfate 30 mg 43885
Ethypharm Inc. M-Elson 60 mg capsule DIN 02019957 Capsule (Extended release) Morphine sulfate 60 mg 43885

Issue

Affected lot may be labeled as M-Eslon 30 mg but may actually contain 60 mg capsules.

What you should do

  • Check your M-Eslon (morphine sulfate) medication bottle or package. If your prescription is for 30 mg, the capsules should be pink and clear. If it contains 60 mg capsules (orange and clear), or if you are unsure, do not take these capsules and contact your pharmacy immediately. Your pharmacist will check the capsules and provide you with a replacement if needed. Return the affected product to your pharmacy for proper disposal.
  • Call 911 immediately and seek immediate medical attention if you or someone you are caring for is experiencing an overdose (e.g., slow breathing, drowsiness, or difficulties waking up).
  • If an overdose is suspected, administer naloxone nasal spray or injection without delay. Give a repeat dose after 2 to 3 minutes if the person has not woken up or their breathing has not improved.
  • Contact your health care professional if you have taken the wrong dose of your medication and have any health concerns.
  • If you have questions about this recall contact Ethypharm Inc. by calling 1-855-694-0151, or by emailing customerservice@valeopharma.com.
  • Report any health product-related side effectsor complaints to Health Canada.

Additional information

Background

Depth of recall: Retailers

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies

Recalling firm:

Valeo Pharma
16667 Hymus Blvd, 
Kirkland, Québec, H9H 4R9

Market authorization holder:

Ethypharm Inc
1200 Avenue McGill College, Suite 1500, 
Montréal, Québec, H3B 4G7

Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type I
Identification number
RA-76224
Media and public enquiries

Media Enquiries:
Health Canada
(613) 957-2983
media@hc-sc.gc.ca

Public Enquiries:
(613) 957-2991
1-866 225-0709
info@hc-sc.gc.ca

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