Philips Medical Systems North America Co. Phillips Interis Allura BiPlane X-Ray System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Interis Allura BiPlane X-Ray System
Brand
Philips Medical Systems North America Co. Phillips
Lot Codes / Batch Numbers
The firm utilizes site numbers: 520582, 531926, 535761, 535775, 520949, 530660, 530654, 522136, 521325, 532241, 531939, 520721, 104949, 530396, 532152, 530653, 532383, 531649, 534756, 533290, 521525, 533397, 534786, 520688, 522456, 520964, 532218, 521149, 520275, 532240, 531758, 520666, 519196, 531799, 519981, 520756, 76992, 534131, 506509, 519197, 533288, 537175, 537181
Products Sold
The firm utilizes site numbers: 520582, 531926, 535761, 535775, 520949, 530660, 530654, 522136, 521325, 532241, 531939, 520721, 104949, 530396, 532152, 530653, 532383, 531649, 534756, 533290, 521525, 533397, 534786, 520688, 522456, 520964, 532218, 521149, 520275, 532240, 531758, 520666, 519196, 531799, 519981, 520756, 76992, 534131, 506509, 519197, 533288, 537175, 537181
Philips Medical Systems North America Co. Phillips is recalling Interis Allura BiPlane X-Ray System due to 1) During positioning of the Lateral Stand the rotation and/or skew movement may travel unexpectedly in opposite direction; 2) movement may be faster . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
1) During positioning of the Lateral Stand the rotation and/or skew movement may travel unexpectedly in opposite direction; 2) movement may be faster than normal speed; 3) the stand may not stop immediately upon release of the joystick.
Recommended Action
Per FDA guidance
A letter issued on 7/25/05 advising customers of problem. The letter advised that an upgrade will be performed.
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