FDA Device recall Z-2010-2019
BrightView X , Model Number 882478
- FDA Device
- Class II
- terminated
- Published 2019-07-31
On 2019-07-31 the FDA classified a Class II recall of BrightView X , Model Number 882478 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-2010-2019 |
| 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 X , Model Number 882478
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: 11000044 11000006 11000033 11000025 11000105 11000016 11000072 11000116 11000101 11000065 110…Serial Numbers: 11000044 11000006 11000033 11000025 11000105 11000016 11000072 11000116 11000101 11000065 11000047 11000018 11000003 11000066 11000078 11000046 11000051 11000114 11000026 11000032 11340001 11000007 11000010 11000027 11000084 11000088 11000057 11000052 11000055 11000068 11000050 11000067 11000070 11000095 11000023 11000102 11000060 11000061 11000094 11000054 11340004 11000091 11000098 11000083 11000063 11000013 11000015 11000062 11000081 11000035 11000009 11000110 11000017 11000090 11000107 11340003 11000056 11000029 11000092 11000041 11000042 11000020 11000109 11000008 11000011 11000039 11000087 11000100 11000093 11000079 11000080 11000074 11000005 11000071 11000043 11000049 11000089 11000030 11000037 11000014 11000104 11000038 11000106 11340002 11000085 11000108 11000040 11000059 11000112 11000045 11000076 11000028 11000113 11000117 11000103 11000069 11000012 11000075 1100 |
|---|
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-2010-2019%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.