au-tgaMedical Device ...

Flixotide and Pavtide Accuhalers

Publicado: 14 de abril de 2026ID de Retiro: 558493Categoría: Dispositivos MédicosPaís: Australia
Australia
Medical DeviceAustraliaAustralia

Flixotide and Pavtide Accuhalers

Recalling Firm: TGA

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Motivo del Retiro / Peligro

GlaxoSmithKline (GSK) Australia Pty Ltd is issuing a product correction for certain batches of their Flixotide and Pavtide Accuhalers as a small number of Accuhalers may not automatically reload the n...

Descripción del Producto e Identificación

GlaxoSmithKline (GSK) Australia Pty Ltd is issuing a product correction for certain batches of their Flixotide and Pavtide Accuhalers as a small number of Accuhalers may not automatically reload the next dose.

Productos Afectados

Flixotide and Pavtide Accuhalers

Additional Source Details

FieldValue
Guid › #texthttps://www.tga.gov.au/node/558493
Guid › @ is Perma Linktrue
Linkhttps://www.tga.gov.au/safety/recalls-and-other-market-actions/market-actions/flixotide-and-pavtide-accuhalers
Pub DateWed, 15 Apr 2026 00:00:00 +1000
Extracted categorydevices

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

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 (issuing safety agency).

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 Flixotide and Pavtide Accuhalers?

Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.

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 (Government Safety Authority). 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 ResponsableTGA
  • Nivel de RiesgoMedical Device Correction
  • DistributionAustralia
Recall Hazard Severity
Caution (Class III)
Alerta Oficial de la Agencia

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🚨 SAFETY ALERT: TGA - Flixotide and Pavtide Accuhalers

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https://therecallfile.com/es/recalls/flixotide-and-pavtide-accuhalers/AU-TGA-558493
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