Recall?

General Discussion on any topic relating to CPAP and/or Sleep Apnea.
Lizzie Dawn
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Location: Albuquerque, NM

Recall?

Post by Lizzie Dawn » Sun Dec 04, 2016 12:45 am

HOW DO I KNOWVIF PARTS OF MY MACHINE HAVE BEEN RECALLED?

AirCurve 10

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kteague
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Location: West and Midwest

Re: Recall?

Post by kteague » Sun Dec 04, 2016 1:27 am

I googled and got lots of hits - not sure about your specific model.

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JDS74
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Re: Recall?

Post by JDS74 » Sun Dec 04, 2016 9:00 am

Lizzie Dawn wrote:HOW DO I KNOWVIF PARTS OF MY MACHINE HAVE BEEN RECALLED?

AirCurve 10
Here is a link to a recall notice for ResMed Canada last year.
http://www.healthycanadians.gc.ca/recal ... 3r-eng.php
the problem seems to be related to the heated hose generating a fault condition as a result of static electricity.

The affected products are:
A. SlimLine
B. AirSense 10 Elite
C. ClimateLine Air
D. AirSense 10 CPAP
E. AirSense 10 AutoSet
F. AirSense 10 AutoSet For Her
G. AirCurve 10 S
H. AirCurve 10 VAuto
I. AirCurve 10 ASV
J. AirCurve 10 ST

In addition, there is a separate recall related to the SERVE-HF clinical study about ASV devices for patients with congestive heart failure. This does not apply to the new S10 devices.

http://www.sleep.org.au/documents/item/1759

The following ResMed devices are affected:
Product Code_____Product Description
25005___________AUTOSET CS
26001___________AUTOSET CS2 - ASIA PACIFIC
26009___________VPAP ADAPT SV - ANZ
36367___________S9 VPAP ADAPT - APAC
36377___________VPAP ADAPT - APAC
37354___________AirCurve 10 CS PaceWave ANZ TRI
25103___________VPAP Tx
36030___________S9 VPAP Tx - APAC

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grayghost4
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Re: Recall?

Post by grayghost4 » Sun Dec 04, 2016 9:17 am

here is a link to the discussion of the static charge problem
It was a very early proplem with the first machines and was corrected with a over the air update of the software

http://www.apneaboard.com/forums/Thread ... ion?page=3
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palerider
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Re: Recall?

Post by palerider » Sun Dec 04, 2016 12:28 pm

JDS74 wrote:In addition, there is a separate recall related to the SERVE-HF clinical study about ASV devices for patients with congestive heart failure. This does not apply to the new S10 devices.
a dispensing advisory is *NOT* a recall.

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