FDA Device recall Z-2011-2019
BrightView XCT , Model Number 882482
- FDA Device
- Class II
- terminated
- Published 2019-07-31
On 2019-07-31 the FDA classified a Class II recall of BrightView XCT , Model Number 882482 by Philips Medical Systems Cleveland, citing an issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2011-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-10 |
| Published | 2019-07-31 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Philips Medical Systems Cleveland |
| Distribution | US |
Product
BrightView XCT , Model Number 882482
Reason
An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.
Identifiers
| code_info | Serial Numbers: 6000241 6000290 6000291 6000292 6000306 6000289 6000304 6000374 6000318 6000219 6000054 6000…Serial Numbers: 6000241 6000290 6000291 6000292 6000306 6000289 6000304 6000374 6000318 6000219 6000054 6000089 6000194 6000165 6000199 6000171 6000053 6000352 6000203 6000396 6000094 6000229 6000391 6000033 6000060 6000220 6000057 6000164 6000167 6000195 6000204 6000235 6000043 6000082 6000295 6000402 6000056 6000237 6000355 6000349 6000317 6000021 6000206 6000026 6000228 6000015 6000163 11000021 6000325 6000022 6000210 6000338 6000012 6000037 6000269 6000047 6000330 6000184 6000128 6000132 6000251 6000310 6000309 6000416 6000077 6000130 6000339 6000066 6000131 6000020 6000147 6000123 6000115 6000126 6000276 6000109 6000081 6000083 6000086 6000246 6000332 6000201 6000036 6000187 6000051 6000351 6000185 6000188 6000084 6000127 6000070 6000183 6000006 6000038 6000045 6000065 6000074 6000380 6000234 6000159 6000334 6000296 6000174 6000173 6000182 6000013 6000113 6000090 6000072 60 |
|---|
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-2011-2019%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.