| Subject: | FDA Publishes Class I Recall Notice for Pulmonetic Systems LTV Ventilators |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 11 Oct 2004 - 10:00 am |
| The FDA has issued a Class I recall of the Pulmonetic Systems LTV series of ventilators due to possible malfunction of the ventilator when switching to the internal battery should an external power source becomes inadequate. The internal battery may malfunction, thus causing failure of the internal battery to allow the ventilator to breathe for the patient. The affected model numbers of ventilators in the Pulmonetic Systems LTV series involved in the recall is:
Model 1000... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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