Stryker Communications: Medical Device Recall in 2025 - (Recall #: Z-2620-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 15, 2025

Date Posted: October 1, 2025

Recall Number: Z-2620-2025

Event ID: 97285

Reason for Recall:

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

Status: Ongoing

Product Quantity: 40

Code Information:

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

Distribution Pattern:

US Nationwide distribution in the states of TX, IL, NY, UT, OR, AZ, VT, NY, IL, MN.

Voluntary or Mandated:

Voluntary: Firm initiated