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Health professional risk communication

Sandoz Morphine Sulfate Injection USP 2mg/mL (1mL) - Some Boxes May Contain Ampoules Labelled as Isoproterenol Hydrochloride Injection - Notice to Hospitals

Starting date:
March 21, 2012
Posting date:
March 21, 2012
Type of communication:
Notice to Hospitals
Subcategory:
Drugs
Source of recall:
Health Canada
Issue:
Contamination
Audience:
Healthcare Professionals
Identification number:
RA-14745

Notice about Health Canada advisories

Notice to Hospitals - Health Canada Issued Important Safety Information on Sandoz Morphine Sulfate Injection USP

March 21, 2012

To: Hospital Chief Pharmacist

Please distribute to all relevant departments and to professional staff and post this notice in your institution.

Subject: Urgent Notice to Hospitals - 2mg/mL (1mL) Sandoz Morphine Sulfate Injection USP - Some boxes may contain ampoules labelled as Isoproterenol Hydrochloride Injection in addition to ampoules labelled as containing morphine

Health Canada is urgently informing healthcare professionals that it has been advised by Sandoz Canada Inc. that one package of 2 mg/mL (1mL) Morphine Sulfate Injection USP has been found to contain ampoules labelled as 0.2 mg/mL (1mL) Isoproterenol Hydrochloride Injection in addition to ampoules labelled as containing morphine.

Sandoz Canada became aware when a hospital reported discovering ampoules labelled as 0.2 mg/mL (1mL) Isoproterenol Hydrochloride Injection USP improperly packaged in a box labeled as containing 2 mg/mL (1mL) ampoules of Morphine Sulfate Injection USP. The box contained ampoules labelled as morphine as well as ampoules labelled as isoproterenol hydrochloride. A photo is provided below and is also available on the Health Canada Web site.

Healthcare professionals are advised to immediately quarantine any supply of products from the lots specified below until further notice.

Inadvertent use of Isoproterenol Hydrochloride Injection USP instead of Morphine Sulfate Injection USP can result in serious health effects. Patients will not receive the intended morphine therapy. As well, isoproterenol hydrochloride is a powerful adrenergic agent. It is associated with a risk of tachycardia and arrhythmia, which may be life threatening. Other side effects may include headache, tremor and sweating.

At this time, Sandoz Canada has indicated to Health Canada that it cannot confirm whether other similar packages exist. Health Canada is working urgently with Sandoz Canada to determine the scope of the issue, and to ensure that other incorrectly packaged product, if any, does not make it into the drug supply system. Health Canada has also informed provinces and territories. New information will be communicated to healthcare professionals as appropriate.

Affected Products:

Morphine Sulfate Injection USP and Isoproterenol Hydrochloride Injection USP

Morphine Sulfate Injection USP

2mg/mL 1mL

DIN 2242484

UPC 057513056420

Lot CC2824 exp. 2014-12

Isoproterenol Hydrochloride Injection USP

0.2 mg/mL 1mL

DIN 897639

UPC 057513046001

Lot CB8787 exp. 2012-11

For health product inquiries related to this communication, please contact Health Canada at:

Health Products and Food Branch Inspectorate

Telephone (toll-free): 1-800-267-9675

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