Z-0344-2009

Allura XPER 10/10

Name: Z-0344-2009 Allura XPER 10/10
Creator: Philips Medical Systems North America Co. Phillips
Published: 2008-12-10
License: https://open.fda.gov/license/

Philips North America LLC / initiated 2008-12-10 / Terminated

FDA source

Philips Medical Systems North America Co. Phillips began a recall of Allura XPER 10/10 on 2008-12-10. The reason FDA records is "Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0344-2009
Status: Terminated
Initiated: 2008-12-10
Posted: 2009-09-24
Terminated: 2012-08-17
Recalling firm: Philips North America LLC
Product: Allura XPER 10/10
Product code: IZI System, X-Ray, Angiographic
Reason for recall: Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.
FDA root cause: Radiation Control for Health and Safety Act
Action: 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
Quantity in commerce: 104 units
Distribution: Worldwide Distribution
Product codes and lots: FCO 72200124 and 72200125 for 1st phase FCO 72200133 for 2nd phase Equipment #'s: 103281, 103283, 505903, 506119, 530653, 532614, 533397, 536028, 536031, 536034, 536035, 536037, 536042, 536171, 536715, 536789, 536899, 537631, 537804, 538028, 538157, 538387, 538409, 538514, 538516, 539326, 539628, 540184, 540237, 541577, 541589, 541590, 542413, 542557, 542714, 543200, 543289, 543411, 543879, 543989, 544395, 544433, 545025, 545396, 545604, 545753, 545884, 545997, 546013, 546569, 547173, 547769, 547823, 547922, 548140, 548288, 549368, 549903, 551855, 554802, 554970, 555293, 555299, 555834, 41443647, 41443804, 41444647, 41444650, 41445448, 41445501, 41445538, 41455885, 41455897, 41455920, 41780160, 42057324, and 42064724. Additional Equipment #s from phase 2- 10107, 101110, 101205, 557729, 557908, 41443609, 41445432, 41446024, 41446262, 41660520, 42046440, 42064058, 42394072, 42553772, 42625859, 42891704, 43043666, 43164789, 43173591, 43453735, 43848923, 43931292, 44028554, 44066424, 44193760, 44892370, and 47140511.

Product code IZI

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)