Philips Medical Systems North America Co. Phillips MultiDiagnost Eleva Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MultiDiagnost Eleva
Brand
Philips Medical Systems North America Co. Phillips
Lot Codes / Batch Numbers
FCO 70800080 Equipment #'s 538440, 544123, 544904, 545156, 545198, 546578, 549417, 551519, 551714, 553287, 553435, 553838, 554283, 554284, 554633, 554640, 556197, 556369, 557258, 41444651, 41445097, 41445127, 41445131, 41445221, 41445237, 41445464, 41445652, 41445800, 41445927, 41455927, 41643223, 41783749, 41849575, 41954854, 42549980, 42799914, 42892004, 42892425, 43319037, 43386703, 43443091, 43453378, 43721197, 44146025, 44401636, and 44653739.
Products Sold
FCO 70800080 Equipment #'s 538440, 544123, 544904, 545156, 545198, 546578, 549417, 551519, 551714, 553287, 553435, 553838, 554283, 554284, 554633, 554640, 556197, 556369, 557258, 41444651, 41445097, 41445127, 41445131, 41445221, 41445237, 41445464, 41445652, 41445800, 41445927, 41455927, 41643223, 41783749, 41849575, 41954854, 42549980, 42799914, 42892004, 42892425, 43319037, 43386703, 43443091, 43453378, 43721197, 44146025, 44401636, and 44653739.
Philips Medical Systems North America Co. Phillips is recalling MultiDiagnost Eleva due to Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.
Recommended Action
Per FDA guidance
An Electronic Product Radiation Warning, dated October 2008, was sent to customers. The letter identified the problem and under what circumstances that it could occur; the actions that should be taken by the customer/user to prevent risks for patients or users; and the actions planned by Philips to correct the problem. Further information or support concerning the issue could be obtained by contacting Bob Pettis at 425-487-7469 or the Philips Call Center at 800-722-9377. Firm FCO tracking numbers 72200107, 72200108, 72200111, 72200112, 72200117, 72200118, 72200119, 72200122, 72200123, 72200124, 72200125, 72200129, 72200142, 7989980, 7080085, 70600034, 70600035, 72200132, 72200133, 72200137, 72200138, 72200140 and 72200141. C & R # 1217116-10/20/08-016C
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