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AED Recalls
| Alert Details for #2004010322 (Released 1/29/2004 12:46 EST) |
| Description: |
Automated External Defibrillators. |
| Manufacturer: |
Access CardioSystems, Concord, MA. |
| Reason: |
Defibrillator may fail to operate due to a faulty component on the circuit board. |
| Alert Type: |
Recall |
Source Alert Type: |
FDA Recall Class II |
| Domain: |
Biomedical Devices |
Source Type: |
FDA Enforcement Report |
| Distribution: |
AL, CA, LA, FL, OR, NC, TN, Grenada |
Source Date: |
1/28/2004 |
| Product Description |
Model/Product Number |
Stock Identifiers |
Volume |
Recall ID |
| Access AED and Access ALS Automated External Defibrillators. |
Model Number: 9100-0100. |
Serial Numbers: 77067, 77341, 77374, 77401, 77427, 77468, 77068, 77344, 77375, 77402, 77428, 77469, 77215, 77351, 77376, 77403, 77429, 77470, 77217, 77352, 77377, 77404, 77430, 77471, 77287, 77353, 77378, 77405, 77432, 77472, 77288, 77354, 77379, 77406, 77433, 77473, 77295, 77355, 77380, 77407, 77434, 77474, 77296, 77356, 77381, 77408, 77435, 77475, 77297, 77357, 77382, 77409, 77436, 77476, 77302, 77358, 77383, 77410, 77437, 77477, 77303, 77359, 77384, 77411, 77438, 77479, 77304, 77360, 77385, 77412, 77439, 77480, 77305, 77361, 77386, 77413, 77440, 77481, 77306, 77362, 77387, 77414, 77441, 77483, 77307, 77363, 77388, 77415, 77442, 77484, 77308, 77364, 77389, 77416, 77443, 77485, 77309, 77365, 77390, 77417, 77444, 77651, 77319, 77366, 77391, 77418, 77445, 77335, 77320, 77367, 77392, 77420, 77446, 77321, 77368, 77394, 77421, 77447, 77334, 77369, 77396, 77422, 77448, 77336, 77370, 77397, 77423, 77462, 77337, 77371, 77398, 77424, 77463, 77338, 77372, 77399, 77425, 77464, 77339, 77373, 77400, 77426, and 77465. |
143 units total. |
Z-0356-04. |
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