FDA Device recall Z-2009-2019
BrightView SPECT, Model Number 882480
- FDA Device
- Class II
- terminated
- Published 2019-07-31
On 2019-07-31 the FDA classified a Class II recall of BrightView SPECT, Model Number 882480 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-2009-2019 |
| 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 SPECT, Model Number 882480
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: 4000665 4000410 4000652 4000651 4000350 4000688 4000224 4000065 4000321 4000002.75 4000044 4…Serial Numbers: 4000665 4000410 4000652 4000651 4000350 4000688 4000224 4000065 4000321 4000002.75 4000044 4000081 4000061 4000180 4000298 4000280 4000229 4000262 4000552 4000378 4000559 4000324 4000576 4000184 4000190 4000516 4000554 4000627 4000566 4000303 4000614 4000411 4000669 4000009 4000305 4000612 4000681 4000301-1 4000202 4000008 4000218 4000166 4000033 4000455 4000287 4000091 4000497 4000498 4000102 4000276 4000123 4000364 4000070 4000699 40000699 4000213 4000012 4000413 4000335 4000197 4000571 4000436 4000648 4000617 4000581 4000500 4000544 4000592 4000491 4000510 4000518 4000472A 4000555 4000454 4000418 4000353 4000469 4000005 4000042 4000379 4000451 4000533 4000602 4000343 4000540 4000547 4000682 4000317 4000338 4000316 4000342 4000408 4000421 4000495 4000511 4000664 4000604 458008 4000647 4000341 4000328 4000375 4000483 4000346 4000683 4000550 4000487 4000039 400060 |
|---|
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-2009-2019%22
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