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Two lots of MAR-Amlodipine Recall

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By RecallRadar Editorial Team

Sourced from Health Canada. Last verified March 4, 2026.

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Key facts

Date announced
February 7, 2026
Source agency
Health Canada

This is a minor issue or quality improvement program.

Plain-English Summary

Two lots of MAR-Amlodipine 5 mg tablets recalle... has been recalled due to a quality issue. Consumers who purchased this product should stop using it immediately. Check the official FDA notice for specific lot numbers and return or disposal instructions.

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

What's Being Recalled

Full details from the recall report.

Recalls and safety alerts

Quick Info

Key facts from the official notice, kept in the article flow for easy cross-checking.

Brand
Fda
Category
medical
Source agency
Health Canada
Announced
February 7, 2026
Country
CA
Status
Active

Who's Affected

Specific model or serial details were not published in this source snapshot. Check the official recall page with your exact model and serial number.

What You Should Do

Follow the remedy path from the official notice using the exact model and serial details above.

  1. 1Immediately check your bottle of MAR-Amlodipine 5 mg tablets.
  2. 2The correct tablets are white to off-white and 8-sided.
  3. 3If your bottle contains any round tablets , return the bottle to your pharmacy for a replacement.
  4. 4Do not take the round tablets.
Open Official Recall Notice

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source
Health Canada
Announced by source
February 7, 2026
Last reviewed by RecallRadar
March 4, 2026

Frequently Asked Questions

Am I affected by this recall?

Check the affected models section on this page. The official notice currently lists FDA products listed in the official notice.

What is the remedy for this recall?

Immediately check your bottle of MAR-Amlodipine 5 mg tablets. The correct tablets are white to off-white and 8-sided. If your bottle contains any round tablets , return the bottle to your pharmacy for a replacement. Do not take the round tablets. Contact your health care professional or call 911 if you are dizzy, have unusually high blood pressure or slow heartbeats. Seek immediate medical attention if you have chest pain, a sudden headache, an inability to move or feel a part of your body, or impaired speech.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://recalls-rappels.canada.ca/en/alert-recall/two-lots-mar-amlodipine-5-mg-tablets-recalled-some-bottles-may-contain-wrong-drug

Keep browsing with these internal hubs: FDA recall hub and Medical recall hub.

Official Resources

Use these primary sources for final eligibility and claim instructions.

View official notice from Health Canada

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