Reported Jul 31, 2019 · Terminated
BrightView SPECT, Model Number 882480
Philips Medical Systems (Cleveland) Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips Medical Systems (Cleveland) Inc · 595 Miner Rd · Cleveland, OH · 44143-2131
Is this the product you have?
- BrightView SPECT, Model Number 882480
- Lot codes and dates
- Serial Numbers4000197_1
137 of 137 codes
4000665400041040006524000651400035040006884000224400006540003214000002.754000044400008140000614000180400029840002804000229400026240005524000378400055940003244000576400018440001904000516400055440006274000566400030340006144000411400066940000094000305400061240006814000301-140002024000008400021840001664000033400045540002874000091400049740004984000102400027640001234000364400007040006994000069940002134000012400041340003354000197
7135_11180 of 180 codes
400012240005494000417400046640001514000389400053640003704000088400029040001584000029400060740006724000286400039540002944000348400061340006554000390400041940004624000463400046440006384222811992884000096400028140002884000484434000597001400027340002684000382400016940004474000595400069240006934000228400044240000474000049400015640004124000297400048840003374000600400058540001094000115400050440006314000494
377 of 377 codes
400044940002164000269400041540003454000208400025440001254000279400062440003074000453400052540005414000289400008740002044000322400001140004034000277400032340002324000668400016040000364000116400040640004894000161400043440000484000241400017740001914000448400059740001714000094400003040005440004704000059400006440005904000104400029240005244000630400014140003614000606400011740006234000138400023940007060008400017640004044000139
- Serial Numbers
- Amount recalled
- 696
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
An issue with the handcontroller may result in either spontaneous uncommanded motions or continued motion after the buttons were released.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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