FDA Medical Device Recalls (openFDA)
Philips Medical Systems North America Co. Phillips: Philips Integris Allura x-ray systems angiographic - Allura 9 F/C (floor and ceiling models). A mono-plane analog Allura with a 9' Image Intensifier
- Recall number
- Z-0366-2007
- Recalling firm
- Philips Medical Systems North America Co. Phillips
- Product
- Philips Integris Allura x-ray systems angiographic - Allura 9 F/C (floor and ceiling models). A mono-plane analog Allura with a 9' Image Intensifier
- Status
- Terminated
- Initiated
- 2006-12-14
- Posted
- 2007-01-25
- Terminated
- 2011-10-14
- Reason
- Movement of the AD5 table or Lateral C-arm (LARC). The table and/or LARC will not move upon request, will move slowly when movement is requested or will not stop moving when requested.
- Root cause
- Other
- Action
- On 12/14/05 and 12/20/06 the firm issued a letter dated 12/12/06 to their customers. The letter explains the problem and states that the firm will be performing mandatory upgrades to correct the situation. Consignees will be contacted to arrange for service.
- Quantity
- 140 devices total
- Distribution
- Units were distributed to hospitals and medical centers nationwide.
- Lot, serial or model codes
- site numbers 534928, 545964, 532207, 545365, 538387, 543397, 543398, 543399, 546572, 544581, 544728, 548147, 547005, 539456, 543953, 547234, 547364, 545838, 545839, 545840, 544395, 547952, 530393, 545799, 540790, 547431, 544122, 541659, 546060, 543433, 545604, 543198, 545921, 545640, 545966, 541590, 540456, 546201, 541572, 544130, 544635, 534665, 542963, 535303, 541783, 544631, 540930, 544610, 544506, 546456, 544989, 544990, 544992, 543984, 543759, 546906, 543873, 543087, 543108, 547279, 546908, 544750, 545518, 545052, 545539, 543799, 543411, 547660, 543229, 544371, 548288, 546668, 545714, 537604, 541046, 544513, 545583, 540808, 545280, 548039, 544489, 544120, 540275, 540284, 540952, 544637, 547855, 545941, 545753, 541597, 545025, 536030, 544543, 546693, 548140, 546025, 545752, 547976, 543971, 543972, 539634, 545749, 546119, 545750, 547642, 544433, 545069, 545073, 547777, 547321, 547628, 545733, 547392, 545293, 545296, 547908, 541880, 543386, 546013, 548061, 545282, 533398, 541588, 541589, 540374, 545357, 542486, 545443, 546012, 545090, 545037, 538432, 532226, 540407, 103281, 104950, 531926, 104953, 530653, 520630
- 510(k) numbers
- ["K002016"]
- PMA numbers
- not on file
- Product code
- IZI
- Firm FEI
- 1000524572
- Firm city
- Bothell
- Firm state
- WA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28