Exact FDA event identifier

Event 66688

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket: October 28, 2013
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Trumpf Medical Systems, Inc.

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

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.

Z-0342-2014

Recall number: Z-0342-2014
Initiated: October 28, 2013
Classification: Class II
Status: Terminated
Recalling firm: Trumpf Medical Systems, Inc.
Quantity: 15 components

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The coupler point (hood) of the Leg Section One Part Light may become detached from the leg section frame.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The coupler point (hood) of the Leg Section One Part Light may become detached from the leg section frame.

Code information

Item no. 1739993, All serial numbers.

Distribution pattern

US Distribution including the states of CA, IL, NJ, NY, NC, TX, WA and SC.