| Subject: | FDA Issues Class I Recall for Welch Allyn AED 10 Automatic External Defibrillators |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 5 Nov 2007 - 02:00 pm |
| Audience: Emergency services personnel, risk managers, and consumersThe FDA has issued a Class I recall for Welch Allyn AED 10 Automatic External Defibrillators manufactured between March 29, 2007 and August 9, 2007, part numbers 970302E, 970308E, 970310E, and 970311E. These devices, used by emergency or medical personnel or by others who have taken the appropriate training in cardiopulmonary arrest, analyze an unconscious patient's heart rhythm and automatically deliver an electrical shock... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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