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

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