CLASS III Device recall · Reported 13 Nov 2013 · FDA Enforcement Report
Orbit PT. The Orbit PT works in conjunction recalled
Trumpf Medical Systems is recalling Orbit PT. The Orbit PT works in conjunction with an Trumpf mobile operating table to, distributed in New Jersey. The recall was initiated on 24 Jul 2013 and the FDA has classified it as Class III.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0155-2014
- FDA event ID
- 66587
- Recalling firm
- Trumpf Medical Systems, Charleston, SC
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 24 Jul 2013
- FDA classified
- 5 Nov 2013
- Reported
- 13 Nov 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 24 Jul 2013 | Recall initiated by company | |
| 5 Nov 2013 | Classified by FDA | +104 days |
| 13 Nov 2013 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column.
Product as listed by the FDA
ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process.
Where it was distributed
US Distribution: NJ only.
Questions about this recall
Why was it recalled?
An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column.
Which lots are affected?
Item No. 1275499, Serial No. 100711351
Where was it sold?
US Distribution: NJ only.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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