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News release

Voluntary Recall of APO-METFORMIN ER (Metformin Hydrochloride Extended-Release Tablets) 500mg Tablets.

Jun 12, 2020

Apotex has initiated a voluntary Type I recall to the Pharmacy Level for nine lots of “APO-METFORMIN ER (Metformin Hydrochloride Extended-Release Tablets) 500mg Tablets”. One lot (PY7174) exceeded the interim acceptable concentration limit for N-nitrosodimethylamine (NDMA) as established by Health Canada. Out of an abundance of caution, an additional eight lots are also being recalled. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables. Consumers should continue taking their metformin drugs, as the risks from not having adequate diabetes treatment far outweigh any possible effects of exposure to the levels of NDMA seen in the recalled products. The details for the nine lots being recalled are listed below:

PRODUCT

DIN

STRENGTH

SIZE/FORMAT

LOT

EXP. DATE (mm/yyyy)

APO-METFORMIN ER (Metformin Hydrochloride Extended-Release Tablets)

02305062

500mg

 

500 BTL

 

PK3968

09/2020

PK3969

09/2020

PX5336

01/2021

PY7174

02/2021

PY7175

01/2021

RF6463

06/2021

RF6464

06/2021

RF6465

06/2021

RF6466

06/2021

APO-METFORMIN ER (Metformin Hydrochloride Extended-Release Tablets) is indicated for the control of hyperglycemia in adult patients with type 2 (non-insulin-dependent, mature onset) diabetes, as an adjunct to dietary management, exercise, and weight reduction, or when insulin therapy is not appropriate. Apo-Metformin ER may be used as monotherapy, or concomitantly with a sulfonylurea. Apo-Metformin ER is a once-daily formulation, which must be taken with food to ensure optimum delivery of metformin to the systemic circulation. Clinical data demonstrates that administration of metformin hydrochloride in the fed state significantly increases the systemic delivery of metformin when compared to the fasted state. Metformin can be of value in the treatment of obese diabetic patients.

To report a suspected adverse reaction associated with the use of APO-METFORMIN ER (Metformin Hydrochloride Extended-Release Tablets) patients may contact Apotex by calling 1-800-667-4708 (select prompt 2), by email at [email protected] or by fax at 1-866-429-9133 or 416-401-3819.

Patients may also report any suspected adverse reactions associated with the use of health products to Health Canada by calling toll free at 1-866-234-2345 or by visiting MedEffect Canada's Web page on Adverse Reaction Reporting https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting.html for information on how to report online, by mail or by fax.

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