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Inogen One G3 Concentrator

Publié le: 27 février 2020ID du rappel: 63e6d6a6-85c8-432b-870d-60ffbb1717e6Catégorie: Produits de ConsommationPays: Australie
Australia
Safety AlertAustralia ProductsAustraliaAustralia

Inogen One G3 Concentrator

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Motif du rappel / Danger

When connected to a fully charged 8-cell battery as its only power source, an operating condition may cause an abrupt shut down of the Inogen One G3 Portable Oxygen Concentrator (POC). If no action is taken, the POC may become unresponsive for up to one minute, after which it will behave as though a battery was just connected with a standard flash screen on display. The POC will then be ready for another startup. If powered on again, this cycle may need to be repeated until the 8-cell battery has been adequately discharged allowing the POC to operate as normal.

Description du produit & Identification

Reason / Defects: When connected to a fully charged 8-cell battery as its only power source, an operating condition may cause an abrupt shut down of the Inogen One G3 Portable Oxygen Concentrator (POC). If no action is taken, the POC may become unresponsive for up to one minute, after which it will behave as though a battery was just connected with a standard flash screen on display. The POC will then be ready for another startup. If powered on again, this cycle may need to be repeated until the 8-cell battery has been adequately discharged allowing the POC to operate as normal. Hazards: Risk of interruption to the supply of oxygen to users, which may lead to health complications. What to do: Customers are advised that arrangements will be made for the products to be repaired and/or replaced. An Air Liquide Healthcare representative will contact customers via phone to initiate the replacement POC, and collect the affected concentrator. For further information, contact Air Liquide Healthcare Customer Service Centre on 1300 360 202.

Produits concernés

Inogen One G3 Concentrator Portable lightweight medical oxygen machine Part Numbers: 19252750, 19252534, 19285707, 19285618, 19285718, 19285621, 19285334, 19252739, 19285727, 19284756, 19252747, 19285626, 19285728, 19252726, 19284685, 19282715, 19285619, 19252733 ARTG 225950 (Air Liquide Healthcare Pty Ltd - Stationary oxygen concentrator)

Additional Source Details

FieldValue
Guid › #text63e6d6a6-85c8-432b-870d-60ffbb1717e6
Guid › @ is Perma Linkfalse
Linkhttps://www.productsafety.gov.au/search-consumer-product-recalls/inogen-one-g3-concentrator
Pub DateThu, 27 Feb 2020 00:00:00 +0000

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 (Australia Products).

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 Inogen One G3 Concentrator?

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 (Australia Products). 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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Aperçu

  • Niveau de risquePharmacy and medical products
  • DistributionAustralia
Recall Hazard Severity
Caution (Class III)
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