Reported Dec 3, 2014 · Terminated
BrightView product code: 882478 BrightView X product code: 882480 BrightView XCT product code: 882482 and 882454
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 product code882478
- BrightView X product code882480
- BrightView XCT product code882482 and 882454
- Lot codes and dates
- BrightView
110000221100002811000050100006711000070110000731000079110000801100008411000088and 11000109
- BrightView X
4000007400003440000454000049400005040000524000055400005740000624000091400011040001194000145400017840001864000192400020340002154000221400023440002674000268400027340003154000332400033540003374000340400034340003494000351400035940003914000404400043640004474000493400049740005004000517400059540005994000605400060940006164000617400062240006484000653and 4000675
- BrightView XCT
600001860000246000025600002960000596000072600007460000966000097600010660001556000170600017960002176000255600025960002726000328600034260003576000388600040560004126340011and 11000082
- BrightView
- Amount recalled
- 85
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Software issues
This product could cause temporary or reversible health problems — stop using it.
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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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