Reported Sep 30, 2026 · Ongoing · Updated Oct 6, 2026

PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Numbers: 1. ARD568474114A, 2.…

Maquet SAS

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: Maquet SAS · Parc De Limere · Orleans Cedex 2 · N/A

Is this the product you have?

  • PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING
  • ARM A2 FC3 50-100nm) Model Numbers
    • 1. ARD568474114A
    • 2. ARD567501286
Lot codes and dates
  • 1
  • Model NumberARD568474114A
  • UDI-DIN/A
  • Serial Numbers

    398 of 398 codes

    • 500190
    • 500194
    • 500201
    • 500203
    • 500209
    • 500216
    • 500218
    • 500197
    • 500204
    • 500210
    • 500211
    • 500212
    • 500213
    • 500214
    • 500217
    • 500206
    • 500390
    • 500393
    • 500397
    • 500414
    • 500416
    • 500417
    • 500418
    • 500451
    • 500266
    • 500284
    • 500291
    • 500293
    • 500294
    • 500299
    • 500300
    • 500301
    • 500302
    • 500306
    • 500307
    • 500308
    • 500117
    • 500116
    • 500273
    • 500274
    • 500399
    • 500400
    • 500402
    • 500168
    • 500188
    • 500192
    • 500196
    • 500208
    • 500219
    • 500221
    • 500228
    • 500233
    • 500237
    • 500240
    • 500247
    • 500159
    • 500207
    • 500215
    • 500396
    • 500415
  • Model NumberARD567501286
  • UDI-DI03700712403478
  • Serial Numbers

    270 of 270 codes

    • 1314H000217400
    • 4014H000279430
    • 4014H000279432
    • 4014H000279433
    • 4014H000279434
    • 4014H000279437
    • 4014H000279438
    • 4314H000288228
    • 4314H000288229
    • 4314H000288232
    • 4314H000288233
    • 4314H000288234
    • 4314H000288237
    • 4314H000288239
    • 4314H000288257
    • 4314H000288258
    • 4314H000288259
    • 4714H000296081
    • 4717H000296095
    • 1315H000382641
    • 1715H000392775
    • 2115H000409030
    • 2115H000409038
    • 2115H000409040
    • 2115H000409062
    • 2113H000123425
    • 3613H000150570
    • 2115H000409063
    • 3015H000436557
    • 3015H000436569
    • 3015H000436571
    • 2115H000409065
    • 2115H000409067
    • 2615H000423256
    • 3015H000436561
    • 3015H000436566
    • 3015H000436570
    • 1314H000215902
    • 1314H000215904
    • 0116H000537022
    • 0716H000208366
    • 2816H000647716
    • 0615H000334882
    • 0615H000334887
    • 0615H000334891
    • 0815H000351763
    • 0815H000351768
    • 0815H000351780
    • 1314H000215893
    • 1314H000215894
    • 1314H000215896
    • 1314H000215900
    • 1314H000215903
    • 1314H000215907
    • 1314H000215885
    • 2114H000236788
    • 2613H000132823
    • 2613H000132825
    • 2613H000132826
    • 2613H000132827
Amount recalled
667

Where it was sold

  • Nationwide

Why it was recalled

The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury.

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

Data as of Nov 4, 4:04 AM 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.