TruSystem Surgical Table — Class II medical device recall Z-0342-2014
Terminated recall by Trumpf Medical Systems, Inc., reported 2013-11-27, distributed in CA, IL, NC, NJ, NY, SC, TX, WA. The coupler point (hood) of the Leg Section One Part Light may become detached from the leg section frame.
| Recall number | Z-0342-2014 |
|---|---|
| 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 | 2013-10-28 |
| Classified | 2013-11-18 |
| Reported by FDA | 2013-11-27 |
| Terminated | 2014-09-16 |
| Distributed | CA, IL, NC, NJ, NY, SC, TX, WA |
| Quantity | 15 components |
| Reason classes | device malfunction |
| Model numbers | 1739993 |
Product
TruSystem Surgical Table (TS7000) Leg Section One Part Light HU Use of the Leg Section One Part Light HU is permitted only with the TRUMPF TruSystem 7000 operating table. The operating table TruSystem 7000, in conjunction with operating table components is intended for the use of patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. The Leg Section One Part Light HU is attached to coupling point L on the operating table and is used to position the patients legs during pre-op and post-op surgery.
Reason for recall
The coupler point (hood) of the Leg Section One Part Light may become detached from the leg section frame.
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-0342-2014. 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.