Reported Jul 31, 2019 · Terminated

BrightView XCT , Model Number 882482

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 XCT , Model Number 882482
Lot codes and dates
  • Serial Numbers

    278 of 278 codes

    • 6000241
    • 6000290
    • 6000291
    • 6000292
    • 6000306
    • 6000289
    • 6000304
    • 6000374
    • 6000318
    • 6000219
    • 6000054
    • 6000089
    • 6000194
    • 6000165
    • 6000199
    • 6000171
    • 6000053
    • 6000352
    • 6000203
    • 6000396
    • 6000094
    • 6000229
    • 6000391
    • 6000033
    • 6000060
    • 6000220
    • 6000057
    • 6000164
    • 6000167
    • 6000195
    • 6000204
    • 6000235
    • 6000043
    • 6000082
    • 6000295
    • 6000402
    • 6000056
    • 6000237
    • 6000355
    • 6000349
    • 6000317
    • 6000021
    • 6000206
    • 6000026
    • 6000228
    • 6000015
    • 6000163
    • 11000021
    • 6000325
    • 6000022
    • 6000210
    • 6000338
    • 6000012
    • 6000037
    • 6000269
    • 6000047
    • 6000330
    • 6000184
    • 6000128
    • 6000132
    7811_12

    148 of 148 codes

    • 6000104
    • 6000231
    • 6000136
    • 6000151
    • 6000180
    • 6000369
    • 6000118
    • 6000080
    • 6000088
    • 6000085
    • 6000244
    • 6000073
    • 6000381
    • 6000393
    • 6000411
    • 6000069
    • 6000011
    • 6000076
    • 6000018
    • 6000092
    • 6000095
    • 6000403
    • 6000313
    • 6000052
    • 6000031
    • 6000107
    • 6000405
    • 6000042
    • 6000153
    • 6000383
    • 6000143
    • 6000117
    • 6000364
    • 6000422
    • 6000160
    • 6000308
    • 6000285
    • 6000112
    • 6000312
    • 6000135
    • 6000172
    • 6000178
    • 6000372
    • 6000019
    • 6000284
    • 6000142
    • 6000340
    • 6000404
    • 6000327
    • 6000198
    • 6000214
    • 6000373
    • 6000387
    • 6000253
    • 6000316
    • 6000063
    • 6000344
    • 6000040
    • 6000394
    • 6000395
Amount recalled
427

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 24, 2020 · Data as of Sep 19, 6:00 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.