Exact FDA event identifier

Event 75115

4 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: July 10, 2016
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

4 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 4

Mobile Column TruSystem 7500, Material Number 1717023; Mobile Column TruSystem 5500, Material Number 1607822 Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recover from the anesthesia. Also, patient transport on the operating table top from a patient transfer system to the operating theater of from the operating theater to a patient transfer system

Z-0040-2017

Recall number: Z-0040-2017
Initiated: July 10, 2016
Classification: Class II
Status: Terminated
Recalling firm: Trumpf Medical Systems, Inc.
Quantity: 84 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

Code information

Serial Numbers - 101281354, 101856082, 101858789, 101858794, 101861232, 101871990, 101871991, 101871994, 101871995, 101871998, 101872002, 101872003, 101875823, 101884649, 101884662, 101890660, 101890661, 101890683, 101895634, 101912771, 101912832, 101912833, 101912837, 101912838, 101916174, 101924149, 101863428, 101875818, 101882033, 101882034, 101882037, 101882038, 101901949, 101901951, 101904490, 101904492, 101907204, 101907205, 101909370, 101909371, 101909372, 101909464, 192052657

Distribution pattern

Worldwide Distribution - US including CA, CT, GA, IL, NC, OR, SC, VA, WI, WY, and Internationally to Australia, Azerbaijan, Brazil, Finland, France, Germany, Hungary, Italy, Luxembourg, Norway, Poland, Russia, Slovakia, and Switzerland

device · product 2 of 4

Stationary Column TruSystem 7599, Material Number 1717020 Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recover from the anesthesia. Also, patient transport on the operating table top from a patient transfer system to the operating theater of from the operating theater to a patient transfer system.

Z-0041-2017

Recall number: Z-0041-2017
Initiated: July 10, 2016
Classification: Class II
Status: Terminated
Recalling firm: Trumpf Medical Systems, Inc.
Quantity: 84 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

Code information

Serial Numbers - 101863421, 101863427, 101863433, 101875827, 101879148, 101879149, 101882031, 101884650, 101884651, 101884653, 101884654, 101890658, 101890659, 101895636, 101904999, 101907202, 101907203

Distribution pattern

device · product 3 of 4

Floor Mounting Column TS 7500 U, Material Number 1730732; Floor Mounting Column ARTIS, Material Number 1501878 Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recover from the anesthesia. Also, patient transport on the operating table top from a patient transfer system to the operating theater of from the operating theater to a patient transfer system.

Z-0042-2017

Recall number: Z-0042-2017
Initiated: July 10, 2016
Classification: Class II
Status: Terminated
Recalling firm: Trumpf Medical Systems, Inc.
Quantity: 84 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

Code information

Serial Numbers - 101900011, 101900018, 101904491, 101904998

Distribution pattern

device · product 4 of 4

Operating Table TruSystem 7000 U, Material Number 1604788; Operating Table TruSystgem 7000 U (MB), Material Number 1604786 Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recover from the anesthesia. Also, patient transport on the operating table top from a patient transfer system to the operating theater of from the operating theater to a patient transfer system

Z-0043-2017

Recall number: Z-0043-2017
Initiated: July 10, 2016
Classification: Class II
Status: Terminated
Recalling firm: Trumpf Medical Systems, Inc.
Quantity: 84 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Three complaints describing TruSystem tables unexpectedly descending approximately 20 centimeters.

Code information

Serial Numbers - 101863316, 101872464, 101879109, 101880571, 101880672, 101880673, 101928935, 101932527, 101937343, 101941055, 101941064, 101941995, 101942798, 101948309, 101954296, 102051758, 102061764, 101926753, 101928934, 101941978, 101941994