Reported Jun 24, 2026 · Ongoing

HarmonyAIR A-Series Surgical Lighting System

Steris Corporation

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: Steris Corporation · 5960 Heisley Rd · Mentor, OH · 44060-1834

Is this the product you have?

  • HarmonyAIR A-Series Surgical Lighting System
Lot codes and dates
  • UDIs

    141 of 141 codes

    • 00724995185947
    • 00724995186418
    • 00724995187156
    • 00724995188009
    • 00724995188498
    • 00724995189198
    • 00724995185954
    • 00724995186425
    • 00724995187170
    • 00724995188016 00724995188504
    • 00724995189211
    • 00724995185961
    • 00724995186432
    • 00724995187187 00724995188047
    • 00724995188535
    • 00724995189228
    • 00724995185978
    • 00724995186548 00724995187217
    • 00724995188054
    • 00724995188542
    • 00724995189280
    • 00724995185985
    • 00724995186555
    • 00724995187248
    • 00724995188078
    • 00724995188580
    • 00724995189372
    • 00724995186067
    • 00724995186562
    • 00724995187262
    • 00724995188122
    • 00724995188597
    • 00724995189419
    • 00724995186074
    • 00724995186579
    • 00724995187279
    • 00724995188221
    • 00724995188603
    • 00724995189990
    • 00724995186081
    • 00724995186593
    • 00724995187286
    • 00724995188238
    • 00724995188610
    • 00724995190002
    • 00724995186098
    • 00724995186616
    • 00724995187347
    • 00724995188245
    • 00724995188627
    • 00724995190033
    • 00724995186111
    • 00724995186623
    • 00724995187378
    • 00724995188252
    • 00724995188634
    • 00724995190040
    • 00724995186128
    • 00724995186661
    • 00724995187385
Amount recalled
2101 units

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

The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

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 Sep 19, 7:35 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.