Health product recall

Ranitidine Injection USP (2020-08-27)

Starting date:
August 27, 2020
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type I
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-73829



Last updated:
2020-08-28

Summary

  • Product:
    Ranitidine Injection USP

Reason

The affected lots may contain particles.

Depth of distribution

Healthcare establishments

Affected products

Ranitidine Injection USP

DIN, NPN, DIN-HIM

DIN 02256711

Dosage form

Solution

Strength

Ranitidine (Ranitidine Hydrochloride) 25 mg/mL

Lot or serial number

JX9941

JS7049

JN6154

JV4206

JV0519

JS1506

JP1270

Companies

Recalling Firm

Sandoz Canada Inc

110 de Lauzon

Boucherville

J4B 1E6

Quebec

CANADA

Marketing Authorization Holder

Sandoz Canada Inc

110 de Lauzon

Boucherville

J4B 1E6

Quebec

CANADA