Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported November 13, 2013
ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process.
An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Trumpf Medical Systems recalled ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to a… - a low-severity action.
ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to a… was recalled by Trumpf Medical Systems in November 13, 2013. Reason: An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller co…. Check the official notice for the remedy. Verify recall #Z-0155-2014 with the FDA Devices before acting.
The recall
Trumpf Medical Systems issued this low-severity FDA Devices recall-An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller co….
- Low
- severity level
- Class III
- classification
- November 13, 2013
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0155-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0155-2014) was formally reported on November 13, 2013, with the manufacturer initiating the action on July 24, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Trumpf Medical Systems is listed as the recalling firm, operating out of Charleston, SC. Federal records list the affected scope as One.
The documented reason for this recall is: An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column. Distribution data in the federal record shows the product reached: US Distribution: NJ only.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
One
Related Recalls
6
3 from same agency
Product description
ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process.
Reason for recall
An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-0155-2014 |
| Date reported | November 13, 2013 |
| Date initiated | July 24, 2013 |
| Recalling firm | Trumpf Medical Systems |
| Firm location | Charleston, SC |
| Affected scope | One |
| Distribution | US Distribution: NJ only. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0155-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
ORBIT PT. The ORBIT PT works in conjunction with an TRUMPF mobile operating table to automate the patient transport process.. Recalled by Trumpf Medical Systems. Units affected: One.
Why was this product recalled? ▼
An odor and smoke developed - The cause was determined to be a power supply unit sitting in the controller column.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 13, 2013. Severity: Low. Recall number: Z-0155-2014.
Where was the recalled product distributed? ▼
Distribution: US Distribution: NJ only..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0155-2014) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported November 13, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.