Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported June 23, 2021
Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat screen monitor. Model: FS32
Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventually detach from the baseplate, result in the display interface dismounti…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Skytron, Div. The Kmw Group, Inc recalled Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket i… - a moderate-severity action.
Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket i… was recalled by Skytron, Div. The Kmw Group, Inc in June 23, 2021. Reason: Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventuall…. Check the official notice for the remedy. Verify recall #Z-1861-2021 with the FDA Devices before acting.
The recall
Skytron, Div. The Kmw Group, Inc issued this moderate-severity FDA Devices recall-Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventuall….
- Moderate
- severity level
- 278 units
- affected scope
- Class II
- classification
- June 23, 2021
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1861-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1861-2021) was formally reported on June 23, 2021, with the manufacturer initiating the action on May 11, 2021. It is classified under Moderate severity (Class II), with a current status of Ongoing. Skytron, Div. The Kmw Group, Inc is listed as the recalling firm, operating out of Grand Rapids, MI. Federal records list the affected scope as 278 units US; 7 units OUS.
The documented reason for this recall is: Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventually detach from the baseplate, result in the display interface dismounting from its attachment point, causing in… Distribution data in the federal record shows the product reached: Worldwide distribution - US Nationwide and the countries of Australia, Japan.. 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
278 units US; 7 units OUS
Related Recalls
6
3 from same agency
Product description
Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat screen monitor. Model: FS32
Reason for recall
Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventually detach from the baseplate, result in the display interface dismounting from its attachment point, causing injury to patients or staff
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1861-2021 |
| Date reported | June 23, 2021 |
| Date initiated | May 11, 2021 |
| Recalling firm | Skytron, Div. The Kmw Group, Inc |
| Firm location | Grand Rapids, MI |
| Affected scope | 278 units US; 7 units OUS |
| Distribution | Worldwide distribution - US Nationwide and the countries of Australia, Japan. |
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-1861-2021) 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? ▼
Skyton Bracket Flatscreen, Revision 2 & 3-The FS32 is a single monitor mounting bracket intended for use with a 32 inch (maximum) flat screen monitor. Model: FS32. Recalled by Skytron, Div. The Kmw Group, Inc. Units affected: 278 units US; 7 units OUS.
Why was this product recalled? ▼
Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventually detach from the baseplate, result in the display interface dismounting from its attachment point, causing injury to patients or staff
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 23, 2021. Severity: Moderate. Recall number: Z-1861-2021.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Japan..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1861-2021) 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 June 23, 2021. 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.