Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 recall (Stryker Communications)
Medical deviceClass IIOngoing
Summary: Stryker Communications is recalling Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001. Reason: Surgical light assembly may not adequate support the weight of the ceiling cover.
What is being recalled
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Why
Surgical light assembly may not adequate support the weight of the ceiling cover.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
Worldwide - US Nationwide distribution.
How to tell if yours is affected
UDI: 07613327296167; All Lots
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1688-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | February 23, 2026 |
| Reported | April 8, 2026 |
| Company | Stryker Communications |
| Company location | Flower Mound, TX, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 6170 units |
More recalls from Stryker Communications · all medical device recalls · recalls from February 2026