healthClass IIRecalled on Oct 1, 2025

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

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Sold At: Stryker Communications(US Nationwide distribution in the states of TX, IL, NY, UT, OR, AZ, VT, NY, IL, MN.)

Recall #: FDA-DEVICE-Z-2620-2025

Source: FDA-ENFORCEMENT

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

Product Identification

Lot/Batch Codes:
UDI-DI: 07613327296167 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

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Summary

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

What to do next

  • 1Stop using this product - may cause temporary or medically reversible health problems
  • 2Check with retailer or manufacturer for recall status and remedy options
  • 3Contact Stryker Communications for return or refund information
  • 4Visit the official FDA recall page for complete details

Summaries only; always follow the official notice.