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Health product recall

Diltiazem-CD 300 mg capsules (2014-02-20)

Starting date:
February 20, 2014
Posting date:
March 14, 2014
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-38223

Recalled products

  1. Diltiazem-CD 300 mg capsules

Reason

This lot is being recalled as a preventative measure because it may not meet dissolution specification limits for its entire shelf life.

Depth of distribution

Wholesalers and pharmacies in Quebec

Affected products

  1. Diltiazem-CD 300 mg capsules

DIN, NPN, DIN-HIM
DIN 02231057
Dosage form

Controlled release capsule

Strength
  • 300 mg
Lot or serial number
  • Lot 13-0307
Companies
Recalling Firm
Pro Doc Ltd.
2925 Industrial Blvd.
Laval
H7L 3W9
Quebec
CANADA
Marketing Authorization Holder
Pro Doc Ltd.
2925 Industrial Blvd.
Laval
H7L 3W9
Quebec
CANADA

Date modified: