Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 28, 2015
TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment rooms, intensive care units, or any area of a medical facility that requires a ceiling mounted device to supply power, medical gases, and data-communication services. TELETOM is designed to be used in rooms that have been constructed to meet National Fire Protection Association.
During the use of the TELETOM Series 4 & 6 there is potential for the controls and brakes not to work properly due to fluid intrusion within the control switches and/or the contro…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Berchtold Corp. recalled TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operat… - a moderate-severity action.
TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operat… was recalled by Berchtold Corp. in October 28, 2015. Reason: During the use of the TELETOM Series 4 & 6 there is potential for the controls and brakes not to work properl…. Check the official notice for the remedy. Verify recall #Z-0154-2016 with the FDA Devices before acting.
The recall
Berchtold Corp. issued this moderate-severity FDA Devices recall-During the use of the TELETOM Series 4 & 6 there is potential for the controls and brakes not to work properl….
- Moderate
- severity level
- 2K units
- affected scope
- Class II
- classification
- October 28, 2015
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0154-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0154-2016) was formally reported on October 28, 2015, with the manufacturer initiating the action on September 23, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Berchtold Corp. is listed as the recalling firm, operating out of Charleston, SC. Federal records list the affected scope as 2129 units.
The documented reason for this recall is: During the use of the TELETOM Series 4 & 6 there is potential for the controls and brakes not to work properly due to fluid intrusion within the control switches and/or the control board assembly. Distribution data in the federal record shows the product reached: Worldwide Distribution - US (nationwide), Canada, and Germany. 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 moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
2129 units
Related Recalls
6
3 from same agency
Product description
TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment rooms, intensive care units, or any area of a medical facility that requires a ceiling mounted device to supply power, medical gases, and data-communication services. TELETOM is designed to be used in rooms that have been constructed to meet National Fire Protection Association.
Reason for recall
During the use of the TELETOM Series 4 & 6 there is potential for the controls and brakes not to work properly due to fluid intrusion within the control switches and/or the control board assembly.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0154-2016 |
| Date reported | October 28, 2015 |
| Date initiated | September 23, 2015 |
| Recalling firm | Berchtold Corp. |
| Firm location | Charleston, SC |
| Affected scope | 2129 units |
| Distribution | Worldwide Distribution - US (nationwide), Canada, and Germany |
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-0154-2016) 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? ▼
TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment rooms, intensive care units, or any area of a medical facility that requires a ceiling mounted device to supply power, medical gases, and data-communication services. TELETOM is designed to be used in rooms that have been constructed to meet National Fire Protection Association.. Recalled by Berchtold Corp.. Units affected: 2129 units.
Why was this product recalled? ▼
During the use of the TELETOM Series 4 & 6 there is potential for the controls and brakes not to work properly due to fluid intrusion within the control switches and/or the control board assembly.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 28, 2015. Severity: Moderate. Recall number: Z-0154-2016.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution - US (nationwide), Canada, and Germany.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0154-2016) 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 October 28, 2015. 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.