Philips Medical Systems North America Co. Phillips MD4 X-ray system Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MD4 X-ray system
Brand
Philips Medical Systems North America Co. Phillips
Lot Codes / Batch Numbers
Site numbers 102550 (20279385), 103023, 38783, 102562 (20279430), 83957, 101155, 82628, 38442, 83038, 13721, 85034, 102583, 80306, 41156, 38993, 84930, X1321, 41032, X1077, 100014, 50328, 17656, 83367, 38586, 100954, 76834, 87176, 41426, 104137, 82800, 103651, 10388, 41111, 17622, 13918, 103377, 101038, X0934, 102034, 52471, 76804, 50251, 44898, 13258, 86545, 101863, 38587, 103043 (20283876), 82688, 38635, 47160, 14099, 45042, 38917, 101156 (20278521), 86328, 38501, 13879, 41439, 41069, 76975, X1277, 100637, X1078, 35484, 101759, 84463, 105022, X1751, 76877, 13172, 38944, 41143, 85694, 87140, 59546, 13704, 10458, 45039, 76869, 52455, 84892, 41271, 87302, 6842, 41031, 41000, X0662, 87030, 76808, 6838, 62938, 86218, 85491, 50340, 82687, 38912, 101153, 103210
Products Sold
Site numbers 102550 (20279385), 103023, 38783, 102562 (20279430), 83957, 101155, 82628, 38442, 83038, 13721, 85034, 102583, 80306, 41156, 38993, 84930, X1321, 41032, X1077, 100014, 50328, 17656, 83367, 38586, 100954, 76834, 87176, 41426, 104137, 82800, 103651, 10388, 41111, 17622, 13918, 103377, 101038, X0934, 102034, 52471, 76804, 50251, 44898, 13258, 86545, 101863, 38587, 103043 (20283876), 82688, 38635, 47160, 14099, 45042, 38917, 101156 (20278521), 86328, 38501, 13879, 41439, 41069, 76975, X1277, 100637, X1078, 35484, 101759, 84463, 105022, X1751, 76877, 13172, 38944, 41143, 85694, 87140, 59546, 13704, 10458, 45039, 76869, 52455, 84892, 41271, 87302, 6842, 41031, 41000, X0662, 87030, 76808, 6838, 62938, 86218, 85491, 50340, 82687, 38912, 101153, 103210
Philips Medical Systems North America Co. Phillips is recalling MD4 X-ray system due to Potential for unexpected table movement.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for unexpected table movement.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026