Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported April 30, 2025
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount
The mounting hardware that is supplied with the 4FXS-60 monitor bracket does not provide adequate thread engagement to support the weight of the frame and monitor. This could lead…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Ihb Operations B.v. recalled Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount - a moderate-severity action.
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount was recalled by Ihb Operations B.v. in April 30, 2025. Reason: The mounting hardware that is supplied with the 4FXS-60 monitor bracket does not provide adequate thread enga…. Check the official notice for the remedy. Verify recall #Z-1663-2025 with the FDA Devices before acting.
The recall
Ihb Operations B.v. issued this moderate-severity FDA Devices recall-The mounting hardware that is supplied with the 4FXS-60 monitor bracket does not provide adequate thread enga….
- Moderate
- severity level
- 112 units
- affected scope
- Class II
- classification
- April 30, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1663-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1663-2025) was formally reported on April 30, 2025, with the manufacturer initiating the action on March 27, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Ihb Operations B.v. is listed as the recalling firm, operating out of Zwolle, N/A. Federal records list the affected scope as 112 units.
The documented reason for this recall is: The mounting hardware that is supplied with the 4FXS-60 monitor bracket does not provide adequate thread engagement to support the weight of the frame and monitor. This could lead to a failure of the mounting hardware a… Distribution data in the federal record shows the product reached: US Nationwide distribution including in the states of AL, AZ, CA, FL, IA, ID, IL, LA, MA, MD, MI, MN, NC, NH, NJ, NM, NY, PA, TN, TX, UT, VA, WI, WV.. 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
112 units
Related Recalls
6
3 from same agency
Product description
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount
Reason for recall
The mounting hardware that is supplied with the 4FXS-60 monitor bracket does not provide adequate thread engagement to support the weight of the frame and monitor. This could lead to a failure of the mounting hardware and subsequent separation of the frame from the mounting column.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1663-2025 |
| Date reported | April 30, 2025 |
| Date initiated | March 27, 2025 |
| Recalling firm | Ihb Operations B.v. |
| Firm location | Zwolle, N/A |
| Affected scope | 112 units |
| Distribution | US Nationwide distribution including in the states of AL, AZ, CA, FL, IA, ID, IL, LA, MA, MD, MI, MN, NC, NH, NJ, NM, NY, PA, TN, TX, UT, VA, WI, WV. |
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-1663-2025) 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? ▼
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount. Recalled by Ihb Operations B.v.. Units affected: 112 units.
Why was this product recalled? ▼
The mounting hardware that is supplied with the 4FXS-60 monitor bracket does not provide adequate thread engagement to support the weight of the frame and monitor. This could lead to a failure of the mounting hardware and subsequent separation of the frame from the mounting column.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 30, 2025. Severity: Moderate. Recall number: Z-1663-2025.
Where was the recalled product distributed? ▼
Distribution: US Nationwide distribution including in the states of AL, AZ, CA, FL, IA, ID, IL, LA, MA, MD, MI, MN, NC, NH, NJ, NM, NY, PA, TN, TX, UT, VA, WI, WV..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1663-2025) 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 April 30, 2025. 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.