Reported Jul 31, 2019 · Terminated
BrightView X , Model Number 882478
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 X , Model Number 882478
- Lot codes and dates
- Serial Numbers
117 of 117 codes
110000441100000611000033110000251100010511000016110000721100011611000101110000651100004711000018110000031100006611000078110000461100005111000114110000261100003211340001110000071100001011000027110000841100008811000057110000521100005511000068110000501100006711000070110000951100002311000102110000601100006111000094110000541134000411000091110000981100008311000063110000131100001511000062110000811100003511000009110001101100001711000090110001071134000311000056110000291100009211000041
- Serial Numbers
- Amount recalled
- 117
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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