Health product recall

TEVA-Betahistine Tablets: Affected lots exceed or may exceed the interim acceptable intake limit for N-nitroso-betahistine.

Last updated

Summary

Product
TEVA-Betahistine Tablets
Issue
Health products - Product safety
What to do

Consult your health care professional if you have any health concerns.

Affected products

Brand Product Name Market Authorization Dosage Form Strength Lot
TEVA-Betahistine Tablets TEVA-Betahistine Tablets 8mg DIN 02280183 Tablet BETAHISTINE HYDROCHLORIDE 8mg 100043755 100047041 100054115 100057407
TEVA-Betahistine Tablets TEVA-Betahistine Tablets 16mg DIN 02280191 Tablet BETAHISTINE HYDROCHLORIDE 16mg 100039202 100039975 100040342 100047037 100047038 100048555 100050930 100052559 100057107 100057408 100058036 100062444 100038357 100047367
TEVA-Betahistine Tablets TEVA-Betahistine Tablets 24mg DIN 02280205 Tablet BETAHISTINE HYDROCHLORIDE 24mg 100038340 100043738 100049891 100052857 100056000 100039609 100039610 100039611 100044222 100049365 100058037

Issue

Affected lots exceed or may exceed the interim acceptable intake limit for N-nitroso-betahistine. 

What you should do

  1. Verify if your product is affected.
  2. Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
  3. Contact the recalling firm if you have any questions about the recall.
  4. Report any health product related side effects to Health Canada.
  5. Report any other health product safety complaints to Health Canada.

Additional information

Background

Depth of recall: Retailers, Pharmacy

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

Teva Canada Limited.

30 Novopharm Court

Toronto, Ontario

M1B 2K9

Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type I
Identification number
RA-76642

Get notified

Receive emails about new and updated recall and safety alerts.

Subscribe