Health CanadaType I

MAR-AMLODIPINE: affected lots may contain tablet(s) of Midodrine 2.5mg tablets.

Publicado: 9 de febrero de 2026ID de Retiro: 81586Categoría: Productos de ConsumoPaís: Canadá
Canada
Safety AlertHealth CanadaCanadaCanada

MAR-AMLODIPINE: affected lots may contain tablet(s) of Midodrine 2.5mg tablets.

Recalling Firm: Drugs and health products

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Motivo del Retiro / Peligro

Product safety

Descripción del Producto e Identificación

Immediately check your medication bottle to ensure it only contains MAR-Amlodipine 5 mg tablets.MAR-Amlodipine 5 mg tablets are white to off-white, flat and eight-sided, with a line across the middle. One side has "210" and "5" printed on it, and the other side is blank.Midodrine 2.5 mg tablets are white, round, and marked with 'M2' on one side and have a line down the middle on the other side.If your bottle contains any unusual tablets or if you are unsure, return it to your pharmacy.If you are unable to get a replacement immediately, continue taking your medication as directed but 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.If you have questions about this recall, contact Marcan Pharmaceuticals Inc. by calling 1-855-627-2261 or by emailing info@marcanpharma.com.Report any health product-related side effects or complaints to Health Canada.Additional information for health professionals:Health care professionals, such as pharmacists, should check packages and bottles labelled MAR-Amlodipine 5 mg (amlodipine besylate) before dispensing to make sure they do not contain midodrine 2.5 mg tablets. Report any unusual bottles or other issues to the company and Health Canada.

Productos Afectados

MAR-AMLODIPINE

Additional Source Details

FieldValue
N I D81586
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/mar-amlodipine-affected-lots-may-contain-tablets-midodrine-25mg-tablets
IssueProduct safety
TitleMAR-AMLODIPINE: affected lots may contain tablet(s) of Midodrine 2.5mg tablets.
ProductMAR-AMLODIPINE
Archived0
CategoryDrugs
Last updated2026-02-09
OrganizationDrugs and health products
Recall classType I
What you should doImmediately check your medication bottle to ensure it only contains MAR-Amlodipine 5 mg tablets.MAR-Amlodipine 5 mg tablets are white to off-white, flat and eight-sided, with a line across the middle. One side has "210" and "5" printed on it, and the other side is blank.Midodrine 2.5 mg tablets are white, round, and marked with 'M2' on one side and have a line down the middle on the other side.If your bottle contains any unusual tablets or if you are unsure, return it to your pharmacy.If you are unable to get a replacement immediately, continue taking your medication as directed but 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.If you have questions about this recall, contact Marcan Pharmaceuticals Inc. by calling 1-855-627-2261 or by emailing info@marcanpharma.com.Report any health product-related side effects or complaints to Health Canada.Additional information for health professionals:Health care professionals, such as pharmacists, should check packages and bottles labelled MAR-Amlodipine 5 mg (amlodipine besylate) before dispensing to make sure they do not contain midodrine 2.5 mg tablets. Report any unusual bottles or other issues to the company and Health Canada.

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Check the model number, serial number, and date stamp on the rating label on the back or underside of the product.

2Isolate & Discontinue Use

Immediately discontinue using the product. Unplug electrical items and keep juvenile items out of reach of children.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (Health Canada).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought MAR-AMLODIPINE: affected lots may contain tablet(s) of Midodrine 2.5mg tablets.?

Immediately stop using the product and keep it out of reach of children. Disconnect power if electrical, and do not attempt makeshift home repairs.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (Health Canada). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Resumen

  • Empresa ResponsableDrugs and health products
  • Nivel de RiesgoType I
Recall Hazard Severity
Caution (Class III)
Alerta Oficial de la Agencia

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