Reported Oct 1, 2025 · Ongoing

Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034

Stryker Communications

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: Stryker Communications · 571 Silveron Blvd · Flower Mound, TX · 75028

Is this the product you have?

  • Chromophare Surgical Light System
  • REFCH00000001; SLX to Oculan NFC Upgrade Kit
  • REFP60034
Lot codes and dates
  • UDI-DI07613327296167
  • and 07613327651317 REF/Serial Numbers
    • CH00000001/7000010116
    • 7000010117
    • 7000010118
    • 7000010119
    • 7000010120
    • 7000010121
    • 7000010122
    • 7000010123
    • 7000010124
    • 7000010125
    • 7000010141
    • 7000010142
    • 7000010177
    • 7000010178
    • 7000010148
    • 7000010149
    • 7000010157
    • 7000010137
    • 7000010175
    • 7000010176
    • 7000010145
    • 7000010146
    • 7000010147
    • 7000010309
    • 7000010305
    • 7000010307
    • 7000010296
    • 7000010143
    • 7000010150
    • 7000010151
    • 7000010155. P60034/1000022
    • 1000023
    • 1000024
    • 1000016
    • 1000017
    • 1000018
    • 1000019
    • 1000020
    • 1000021
Amount recalled
40

Where it was sold

Why it was recalled

Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.

This product could cause temporary or reversible health problems — stop using it.

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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, 5:43 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.