Device recalls

Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Software Version Number 8.1.100.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected m…

Open, ClassifiedUnder Investigation by firmZ-1897-2024
Open FDA's page for this record
Cfres ID
207941
Product res number
Z-1897-2024
Event date initiated
2024-05-16
Event date posted
2024-05-24
Recall status
Open, Classified
Res event number
94647
Product code
OWB
Product description
Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Software Version Number 8.1.100.
Code info
Product number: 722013, UDI/DI: 00884838059061; Serial Number: 232.
Firm FEI number
3002807880
Recalling firm
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Address 1
Veenpluis 4-6 4-6 veenpluis
City
Best
Country
Netherlands
Additional info contact
Virginia Huete 31-615-679227
Root cause description
Under Investigation by firm
Product quantity
1 unit (OUS)
Distribution pattern
Domestic: OK International: India, Spain, U.A.E.
Reason for recall

When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.

Action

On May 14, 2024 URGENT Medical Device Correction letters were sent to consignees. Actions that should be taken by the customer / user to lower risks for patients: " Circulate this Urgent Medical Device Correction letter to all users so that they are aware of the issue. " Philips recommends discontinuing use of the system for procedures that can be safely postponed to another time, or for procedures that can be performed with another system. " Keep this Urgent Medical Device Correction letter with the documentation of the system until Philips corrects your system. Ensure the letter is in a place likely to be seen/viewed. " Please complete and return the attached response form (on page 3) to Philips promptly and no later than 15 days from receipt. Completing this form confirms receipt of the Medical Device Correction letter and understanding of the issue and required actions to be taken. 5. Actions planned by Philips IGT-S to correct the issue: Philips will be re-installing the previous software release in all affected systems. Philips will contact affected customers immediately to schedule a visit to perform this software change (reference FCO72200588). If you need additional information or support concerning this issue, please contact your local Philips representative at 1-800-722-9377 (Philips Customer Care Solutions Center).

K numbers
K162859
Harmonized identifiers (openFDA)
Device name
Interventional Fluoroscopic X-Ray System
Medical specialty description
Radiology
Regulation number
892.1650
Device class
2
K number
K243735, K170130, K253670, K221344, K220342, K173631, K180473, K243884, K211191, K200917, K050489, K211780, K212442, K231700, K101868, K181550, K173314, K251523, K163715, K123508, K181804, K240465, K032046, K231669, K130638, K172646, K062647, K203281, K052202, K181834, K002198, K212383, K033244, K230787, K160147, K961374, K123529, K181415, K222625, K233230 +285 more
Registration number
3021059265, 3016438694, 3014391847, 2027467, 3038614464, 3010398867, 9681146, 3004785967, 3015223550, 3009196578, 3008632256, 3003202425, 3012761544, 1723170, 3001722928, 2243057, 3003768251, 3021561977, 3010703925, 3036666444, 3021027284, 3013184485, 3022378058, 3008284470, 3011713200, 3027373189, 3036255956, 3018094310, 8030233, 3006544299, 3016248538, 1225677, 3009973505, 1037955, 2133772, 3008363989, 3025394757, 2939520, 3030412764, 3014343100 +86 more
FEI number
3021059265, 3016438694, 1000114111, 3014391847, 2027467, 3038614464, 3002808139, 3010398867, 3004785967, 3015223550, 3009196578, 3008632256, 3003202425, 3012761544, 3001722928, 2243057, 3002980729, 3003768251, 3021561977, 3010703925, 3036666444, 3021027284, 3013184485, 3022378058, 3008284470, 3011713200, 3027373189, 3036255956, 3018094310, 3006544299, 3016248538, 3009973505, 1037955, 1000132370, 3008363989, 3025394757, 2939520, 3030412764, 3014343100, 1000188474 +86 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.