Reported Oct 29, 2014 · Terminated

Esprit V1000 and V200 Ventilators, Model No. V1000 and V200; and the 3rd Generation Power Supply Repair Part (RP)Kits…

Respironics California Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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: Respironics California Inc · 2271 Cosmos Ct · Carlsbad, CA · 92011-1517

Is this the product you have?

  • Esprit V1000 and V200 Ventilators, Model No. V1000 and V200; and the 3rd Generation Power Supply Repair Part (RP)Kits Microprocessor-controlled, electrically powered mechanical ventilators intended for use by qualified medical personnel to provide continuous or intermittent ventilator support for adult, pediatric and neonatal patients as prescribed by a physician.
Lot codes and dates
  • Serial Numbers

    665 of 665 codes

    • VS0002577
    • VS0002579
    • VS0002580
    • VS0002581
    • VS0002583
    • VS0002584
    • VS0002585
    • VS0002586
    • VS0002587
    • VS0002588
    • VS0002589
    • VS0002590
    • VS0002593
    • VS0002595
    • VS0002596
    • VS0002599
    • VS0002602
    • VS0002603
    • VS0002604
    • VS0002605
    • VS0002606
    • VS0002609
    • VS0002610
    • VS0002611
    • VS0002613
    • VS0002615
    • VS0002616
    • VS0002625
    • VS0002630
    • VS0002746
    • VS0002750
    • VS0002752
    • VS0002753
    • VS0002759
    • VS0002728
    • VS0002773
    • VS0002765
    • VS0002772
    • VS0002828
    • VS0002842
    • VS0002830
    • VS0002834
    • VS0002859
    • VS0002873
    • VS0002874
    • VS0002877
    • VS0002879
    • VS0002884
    • VS0002844
    • VS0002846
    • VS0002847
    • VS0002851
    • VS0002856
    • VS0002891
    • VS0002815
    • VS0002816
    • VS0002924
    • VS0002927
    • VS0002929
    • VS0002932
  • International Serial Numbers

    1,541 of 1,541 codes

    • VS0002612
    • VS0002600
    • VS0002601
    • VS0002628
    • VS0002635
    • VS0002637
    • VS0002638
    • VS0002696
    • VS0002697
    • VS0002699
    • VS0002701
    • VS0002702
    • VS0002619
    • VS0002620
    • VS0002641
    • VS0002695
    • VS0002703
    • VS0002704
    • VS0002706
    • VS0002707
    • VS0002700
    • VS0002709
    • VS0002647
    • VS0002713
    • VS0002714
    • VS0002715
    • VS0002718
    • VS0002717
    • VS0002724
    • VS0002730
    • VS0002732
    • VS0002745
    • VS0002747
    • VS0002748
    • VS0002743
    • VS0002716
    • VS0002723
    • VS0002731
    • VS0002754
    • VS0002755
    • VS0002758
    • VS0002760
    • VS0002761
    • VS0002762
    • VS0002763
    • VS0002767
    • VS0002757
    • VS0002764
    • VS0002766
    • VS0002780
    • VS0002784
    • VS0002785
    • VS0002786
    • VS0002788
    • VS0002790
    • VS0002779
    • VS0002792
    • VS0002793
    • VS0002794
    • VS0002798
Amount recalled
2,206 units total (665 units in US)

Why it was recalled

Stop using this product now

A failure of a specific component may prevent the ventilators from operating on AC power or transitioning back to AC power when operating on battery. Additionally, if a battery is not present or is depleted the ventilators will not operate. This failure will cause the loss of ventilator support, which may result in hypercarbia or hypoxemia.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 28, 2016 · Data as of Sep 19, 5:35 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.