Health product recall

Thiamiject Injection (2019-11-06)

Starting date:
November 6, 2019
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-71579

Last updated: 2019-11-12

Summary

  • Product: Thiamiject Injection - Liq IM IV 100 mg/mL

Reason

The assay is out of specification in the affected lots.

Depth of distribution

Wholesalers, Healthcare Establishments, Retailers

Affected products

Thiamiject Injection - Liq IM IV 100 mg/mL

DIN, NPN, DIN-HIM

DIN 02193221

Dosage form

Liquid

Strength

Thiamine hydrochloride 100 mg/mL

Lot or serial number

7K940, 7M997, 8G265, 8K328, 9A435A, 9A435B

Companies

Recalling Firm
Omega Laboratories Ltd.
11177 Hamon
Montreal
H3M 3E4
Quebec
CANADA
Marketing Authorization Holder
Omega Laboratories Ltd.
11177 Hamon
Montreal
H3M 3E4
Quebec
CANADA