Trumpf Ceiling Mounted Surgical Lighting Systems — Class II medical device recall Z-2357-2015
Terminated recall by Trumpf Medical Systems, Inc., reported 2015-08-19, distributed nationwide. Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.
| Recall number | Z-2357-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Trumpf Medical Systems, Inc., Charleston, SC, United States |
| Recall initiated | 2015-07-27 |
| Classified | 2015-08-07 |
| Reported by FDA | 2015-08-19 |
| Terminated | 2017-05-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AT, AU, BE, BG, BH, CA, CH, CL, CN, CY, CZ, DE, DK, EC, EE, EG, ES, FI, FR, GB, GR, HK, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JO, JP, KE, KR, KW, LB, LT, LU, LV, MA, MT, MX, MY, NL, NO, NZ, PE, PH, PK, PL, PT, QA, RO, RS, RU, SA, SE, SG, SI, SK, TH, TN, TR, TW, UA, UY, VE, VN, ZA |
| Quantity | 9,287 units |
| Reason classes | device malfunction |
Product
Trumpf Ceiling Mounted Surgical Lighting Systems,TruVidia HD, User Manual #1513140. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
Reason for recall
Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.
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-2357-2015. 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.