Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling… — Class II medical device recall Z-0563-2016
Completed recall by Trumpf Medical Systems, Inc., reported 2016-01-06, distributed nationwide. The firm has received 15 complaints over ten years related to the connection of the spring arm to the top hori
| Recall number | Z-0563-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Trumpf Medical Systems, Inc., Charleston, SC, United States |
| Recall initiated | 2015-11-02 |
| Classified | 2015-12-31 |
| Reported by FDA | 2016-01-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 20,713 |
Product
Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5
Reason for recall
The firm has received 15 complaints over ten years related to the connection of the spring arm to the top horizontal arm of the lighting system that while positioning the light head enabled the spring arm and light head to fall.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0563-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.