FDA Device Recalls

Recalls /

#179836

Product

Cardio Vascular-Allura Centron, system code 722400

FDA product code
OWBInterventional Fluoroscopic X-Ray System
Device class
Class 2
Medical specialty
Radiology
510(k) numbers
K141979
Affected lot / code info
Not distributed in US. Serial numbers 132 133 49 66 71 135 31 36 79 69 137 149 147 109 136 108 103 93 53 127 129 129 55 74 2 57 106 56 86 68 157 78 64 63 23 51 100 97 102 113 90 44 30 101 77 83 67 151 22 70 96 116 131 35 82 9 91 43 61 161 28 34 27 19 144 92 168 172 173 122 197 139 6 76 176 16 130 60 80 184 112 81 89 42 110 155 33

Why it was recalled

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.

Root cause (FDA determination)

Component design/selection

Action the firm took

On 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.

Recalling firm

Firm
Philips North America, LLC
Address
3000 Minuteman Rd, Andover, Massachusetts 01810-1032

Distribution

Distribution pattern
Nationwide domestic distribution. Foreign distribution worldwide.

Timeline

Recall initiated
2019-12-30
Terminated
2022-11-17
Status

Source: openFDA Device Recall endpoint. Recall record ID #179836. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.