FDA Device recall Z-1489-2020

MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038

FDA Device
Class II
terminated
Published 2020-03-25

On 2020-03-25 the FDA classified a Class II recall of MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038 by Philips North America, citing 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.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1489-2020
Classification	Class II
Status	terminated
Initiated	2019-12-30
Published	2020-03-25
Last updated	2026-09-13 11:55 UTC
Company	Philips North America
Distribution	US

Product

MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038

Reason

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.

Identifiers

code_info	Serial Codes 32 177 98 18 42 40 239 228 123 235 152 107 90 26 239 272 88 258 52 111 67 111… Serial Codes 32 177 98 18 42 40 239 228 123 235 152 107 90 26 239 272 88 258 52 111 67 111 85 257 46 94 129 142 121 172 191 41 143 185 36 129 32 81 136 120 159 236 114 113 181 109 124 244 238 23 82 65 57 91 15A 249 259 74 207 101 182 101 174 70 124 34 138 188 142 86 35 37 128 47 118 4 178 158 172 27 43 117 148 149 10 45 203 79 47 229 151 7 5 24 64 184 183 76 173 58 199 29 119 34 407 126 524617 152 188 71 52 60 242 244 52 393 346 49 102 47 197 198 34 147 87 134 178 237 105 176 190 241 397 36 245 13 187 175 38 162 107 76 220 65 15 26 194 81 126 217 69 124 184 107 139 35 13 15 373 66 215 78 241 25 50 112 150 86 230 22 42 145 12 207 206 29 139 98 222 146 79 29 151 111 158 61 33 106 190 35 50 17 16 80 59 S01H044631 S01H055478 METRA01139 4.5161E+15 62 70 228 376 77 8 76 59 88

code_info

Serial Codes 32 177 98 18 42 40 239 228 123 235 152 107 90 26 239 272 88 258 52 111 67 111…

Serial Codes 32 177 98 18 42 40 239 228 123 235 152 107 90 26 239 272 88 258 52 111 67 111 85 257 46 94 129 142 121 172 191 41 143 185 36 129 32 81 136 120 159 236 114 113 181 109 124 244 238 23 82 65 57 91 15A 249 259 74 207 101 182 101 174 70 124 34 138 188 142 86 35 37 128 47 118 4 178 158 172 27 43 117 148 149 10 45 203 79 47 229 151 7 5 24 64 184 183 76 173 58 199 29 119 34 407 126 524617 152 188 71 52 60 242 244 52 393 346 49 102 47 197 198 34 147 87 134 178 237 105 176 190 241 397 36 245 13 187 175 38 162 107 76 220 65 15 26 194 81 126 217 69 124 184 107 139 35 13 15 373 66 215 78 241 25 50 112 150 86 230 22 42 145 12 207 206 29 139 98 222 146 79 29 151 111 158 61 33 106 190 35 50 17 16 80 59 S01H044631 S01H055478 METRA01139 4.5161E+15 62 70 228 376 77 8 76 59 88

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1489-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.