Severity
Moderate
FDA Devices recall · Reported June 28, 2017
Elevating Monitor Suspension column dropping and will not rise back up.
Omega Medical Imaging, Inc. recalled Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension pillar/column accessory … - a moderate-severity action.
Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension pillar/column accessory … was recalled by Omega Medical Imaging, Inc. in June 28, 2017. Reason: Elevating Monitor Suspension column dropping and will not rise back up.. Check the official notice for the remedy. Verify recall #Z-2621-2017 with the FDA Devices before acting.
The recall
Omega Medical Imaging, Inc. issued this moderate-severity FDA Devices recall-Elevating Monitor Suspension column dropping and will not rise back up..
Sourced from official FDA Devices enforcement records. Verify recall #Z-2621-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Devices action (record #Z-2621-2017) was formally reported on June 28, 2017, with the manufacturer initiating the action on March 23, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Omega Medical Imaging, Inc. is listed as the recalling firm, operating out of Sanford, FL. Federal records list the affected scope as 6 units.
The documented reason for this recall is: Elevating Monitor Suspension column dropping and will not rise back up. Distribution data in the federal record shows the product reached: Worldwide Distribution -US Distribution to states of: IN, OH, PA, and MT; and country of: Pakistan.. 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.
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.
Severity
Moderate
Affected scope
6 units
Related Recalls
6
3 from same agency
Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension pillar/column accessory Device accessory that elevates monitor for healthcare professionals.
Elevating Monitor Suspension column dropping and will not rise back up.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2621-2017 |
| Date reported | June 28, 2017 |
| Date initiated | March 23, 2017 |
| Recalling firm | Omega Medical Imaging, Inc. |
| Firm location | Sanford, FL |
| Affected scope | 6 units |
| Distribution | Worldwide Distribution -US Distribution to states of: IN, OH, PA, and MT; and country of: Pakistan. |
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.
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.
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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 28, 2017. 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.