Stryker CHROMOPHARE Softlit Ring Surgical Light Recall: Ceiling Support Risk

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Contact the company & request your remedy

Recalling firmStryker Communications571 Silveron Blvd · Flower Mound, TX 75028

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Stryker is recalling its CHROMOPHARE Softlit Ring Surgical Light System because the assembly might not support the ceiling cover's weight. This could lead to the light falling and causing injury during surgery.

Why it’s dangerous

The surgical light assembly may not hold the ceiling cover securely. If the ceiling cover becomes unstable, the light could fall and cause injury during surgery.

Who’s affected

Surgical teams using the CHROMOPHARE Softlit Ring Surgical Light System are most at risk. Patients and staff could be injured if the light falls.

How to tell if you have this one

Check for the product name 'CHROMOPHARE Softlit Ring Surgical Light System' and reference number CH00000001. All units are affected regardless of purchase date.

Brand
Stryker
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Current Use
Ensure the light is securely attached to the ceiling cover before use.
Verify Product Details
Look for the reference number CH00000001 on the product label.

✎ GovInfoNow

Questions people ask

Is this recall affecting all units?

Yes, all units of the CHROMOPHARE Softlit Ring Surgical Light System with reference number CH00000001 are affected.

How can I tell if my light is recalled?

Check for the reference number CH00000001 on the product label. All units are affected regardless of when they were purchased.

What should I do if the light falls?

The recall record does not specify actions for this scenario.

Take action

Contact Stryker

We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1688-2026 — Stryker Stryker

Hello,

I own a Stryker that is covered by recall Z-1688-2026 from Stryker.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1688-2026 (February 23, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1688-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001

Use caution until it’s fixed