JAMP Digoxin 0.0625 mg and 0.125 mg tablets recalled due to possible incorrect dose, which may pose health risks
Why it was recalled
Product safety
What you should do
If you are taking this medication, speak with your pharmacist as soon as possible. Your pharmacist will check if your product is affected and provide a replacement if needed. It may not be possible to know if you are getting the correct dose of digoxin by looking at the tablets. Overweight or underweight tablets may look like normal-sized tablets.Continue taking your JAMP Digoxin 0.0625 or 0.125 mg tablets until you speak with your pharmacist, as digoxin is an important drug when you have a heart condition.Contact a health care professional immediately if you or someone you are caring for experience serious side effects related to an overdose of digoxin or reduced efficacy of therapy.Contact JAMP Pharma Corporation by calling toll-free at 1-866-399-9091, extension 501, or by email at custjamp@jamppharma.com, if you have questions about this recall.Report any health product-related side effects or complaints to Health Canada.
Other Recent Recalls
Apo-Semaglutide Injection
Apo-Semaglutide Injection : Incorrect dose display
Moderate health risk
Novo-Gesic Forte 500 mg tablets (acetaminophen)
Generic acetaminophen by Teva recalled because it may contain foreign material
Highest health risk
JAMP Temozolomide
JAMP Temozolomide: Out-of-Specification (Assay)
Moderate health risk
Recall data is sourced from Health Canada's Recalls and Safety Alerts open dataset. MedShort.ca is an independent tracking tool and does not provide medical advice — for questions about this recall, contact the manufacturer or your pharmacist, or read the full notice linked above.