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New Search Back To Search Results   Medical Device Recalls Class 2 Recall MD 4 Date Recall Initiated April 06, 2006 Date Posted May 06, 2006 Recall Number Z-0852-06 Product MD4 X-ray system Code Information Site numbers 52459, 38929, 41378, 20279385, 38783, 20279430, 83957, 82628, 83038, 13721, 85034, 80306, 38993, 84930, X1321, X1077, 44812, 100014, 50328, 17656, 83367, 38586, 76834, 87176, 41426, 82800, 10388, 41111, 17622, 13918, 84854, 102034, 38202, 52471, 76804, 50251, 44898, 13258, 86545, 38587, 20283876, 82688, 38635, 47160, 45042, 38917, 20278521, 86328, 13879, 41069, 76975, X1277, X1078, 76951, 84463, 76877, 13172, 38944, 41143, 85694, 87140, 59546, 13704, 45039, 20280426, 76869, 52455, 84892, 41271, 87302, 6842, 41031, 6825, X0662, 87030, 76808, 6838, 86218, 85491, 50340, 82687, 38912, 41287, 41000, 100700, 41439, 41156, 10458, 35484, 103056, X0934, 38501, 14099, 62938 Recalling Firm/ Manufacturer Philips Medical Systems North America Co. Phillips 22100 Bothell Everett Hwy Bothell , Washington 98021-8431 For Addition Information Contact Sarah Baxter 425-487-7665 Reason For Recall Potential for unexpected table movement. Action On 4/6/06 the firm issued a letter to consignees advising of the problem. The letter advises consignees to conduct a test on their unit(s) for a possible short until the firm is able to upgrade the units. . Quantity in Commerce 94 units Distribution Units were distributed to hospitals and medical centers located throughou the US.

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