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U.S. Department of Health and Human Services

Class 2 Device Recall Integris Allura 15 & 12 Interventional fluoroscopic xray system

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 Class 2 Device Recall Integris Allura 15 & 12 Interventional fluoroscopic xray systemsee related information
Date Initiated by FirmDecember 30, 2019
Create DateMarch 13, 2020
Recall Status1 Terminated 3 on November 17, 2022
Recall NumberZ-1487-2020
Recall Event ID 84756
510(K)NumberK002016 
Product Classification Interventional fluoroscopic x-ray system - Product Code OWB
ProductIntegris Allura 15 & 12, monoplane (system code 722043) and biplane (system code 722044)
Code Information Serial Codes  3217017 200 58 72 CV.170 180 524615 47 211 364 30 3862570/0011 529 S.N. 519 S01H060871 505/0050114 S01H057274 01H077213 530 532 S01HA52566 348 476 320 481 467 284 352 359 459 73*004 733 536 CV.474 454 49 281 51 186 122 250 37 22 CV.312 296 373 CV.596 176 30 580 279 
Recalling Firm/
Manufacturer		 Philips North America, LLC
3000 Minuteman Rd
Andover MA 01810-1032
For Additional Information ContactTechnical Support Line
800-722-9377
Manufacturer Reason
for Recall		A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.
FDA Determined
Cause 2		Component design/selection
ActionOn December 30, 2019, the firm notified customers via Medical Device Correction letter. Customers were informed of the product issue and advised to do the following: If the capacitor of the Velara X-Ray fails as described (capacitor failure after large number of surges in a short period of time), please switch off the system, take it out of service immediately, and contact your local Philips representative. The firm will be resolving the issue by replacing a Printed Circuit Board (PCB) in the convertor, which prevents the capacitor from failing. PCB replacements started in January 2020. Customers will be contacted by their local Philips representatives to schedule a date for the PCB replacement. Customers with further questions should contact the Technical Support Line: 1-800-722-9377.
Quantity in Commerce70
DistributionNationwide domestic distribution. Foreign distribution worldwide.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = OWB
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