Acrobat 3000 — Class II medical device recall Z-2311-2012
Terminated recall by Trumpf Medical Systems, Inc., reported 2012-09-12, distributed in CA, NY, OH, OK, PA, TX, WY. Cracks can arise on the welded seam on the rear joint.
| Recall number | Z-2311-2012 |
|---|---|
| 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 | 2012-05-29 |
| Classified | 2012-09-05 |
| Reported by FDA | 2012-09-12 |
| Terminated | 2013-04-11 |
| Distributed | CA, NY, OH, OK, PA, TX, WY |
| Countries outside the US | CA |
| Quantity | 402 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00011207603314 |
| Serial numbers | 011201602557, 011201602588, 011202602621, 011203602617, 011203602676, 011203602695, 011203602756, 011203602775, 011203602776, 011203602795, 011204602798, 011204602817, 011204602861, 011204602880, 011204602970, 011204602989, 011205603032, 011205603081, 011205603333, 011206603118, 011206603167, 011206603168, 011206603217, 011207603303, 011207603314 and 10 more |
Product
Acrobat 3000 (AC3000) Spring Arm as support arm for iLED operating lights, TRUMPF Medizinsysteme GmbH + Co KG 82178 Puchheim. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.
Reason for recall
Cracks can arise on the welded seam on the rear joint.
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-2311-2012. 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.