Z-1494-2020 Class II Terminated

Recalled by Philips North America, LLC — Andover, MA

Recall Details

Product Type
Devices
Report Date
March 25, 2020
Initiation Date
December 30, 2019
Termination Date
November 17, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
87

Product Description

Cardio Vascular-Allura Centron, system code 722400

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.

Distribution Pattern

Nationwide domestic distribution. Foreign distribution worldwide.

Code Information

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