Reported Feb 10, 2016 · Terminated

Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for…

Resmed Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Resmed Corporation · 9001 Spectrum Center Blvd · San Diego, CA · 92123-1438

Is this the product you have?

    • Astral 100
    • 150
  • Model27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for example, the largest population of patients on the Astral device is COPD patients primarily using the device at night with some daytime use for recovery breathing. While it is possible that there may be scenarios where critically dependent patients may encounter this scenario, the likelihood of this leading to harm is negligible because critically dependent patients will have a form of backup ventilation as standard of care
Lot codes and dates
  • Serial Numbers

    2,507 of 2,507 codes

    • 22141311907
    • 22151237236
    • 22141311910
    • 22151237228
    • 22151572231
    • 22151666684
    • 22151237233
    • 22151135073
    • 22141458006
    • 22151572230
    • 22151135061
    • 22151397090
    • 22151008941
    • 22141311872
    • 22151614456
    • 22151135058
    • 22141269867
    • 22151555593
    • 22151483516
    • 22151483534
    • 22151325490
    • 22151163315
    • 22141308812
    • 22151555584
    • 22151311349
    • 22141311870
    • 22151602423
    • 22151325513
    • 22151555618
    • 22151165427
    • 22151165476
    • 22151468419
    • 22151397046
    • 22151073624
    • 22151165376
    • 22151602615
    • 22151445731
    • 22151326787
    • 22151483592
    • 22151602601
    • 22151165492
    • 22151555637
    • 22151311317
    • 22151608382
    • 22151608488
    • 22151310708
    • 22151326727
    • 22151165536
    • 22151468487
    • 22151165539
    • 22151503647
    • 22151310704
    • 22151602504
    • 22141311844
    • 22151572224
    • 22151503641
    • 22151399554
    • 22141668174
    • 22151468486
    • 22151397041
Amount recalled
14,736

Where it was sold

Why it was recalled

Resmed Corporation is recalling Astral 100, 150 External Battery because of a start-up issue.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 22, 2016 · Data as of Sep 19, 6:00 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.