CLASS II Device recall · Reported 28 Jun 2017 · FDA Enforcement Report

2 over 2 Elevating Monitor Suspension pillar/column recalled

Omega Medical Imaging is recalling 2 over 2 Elevating Monitor Suspension pillar/column accessory Device accessory that, distributed in Indiana, Montana, Ohio, Pennsylvania. The recall was initiated on 23 Mar 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSKF Telescopic Pillar P/N ending in -003

Quantity recalled6 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2621-2017
FDA event ID: 77458
Recalling firm: Omega Medical Imaging, Sanford, FL
Classification: Class II
Status: Terminated
Recall initiated: 23 Mar 2017
FDA classified: 22 Jun 2017
Reported: 28 Jun 2017
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Imaging Equipment

Timeline

23 Mar 2017	Recall initiated by company
22 Jun 2017	Classified by FDA	+91 days
28 Jun 2017	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Elevating Monitor Suspension column dropping and will not rise back up.

Product as listed by the FDA

Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension pillar/column accessory Device accessory that elevates monitor for healthcare professionals.

Where it was distributed

Worldwide Distribution -US Distribution to states of: IN, OH, PA, and MT; and country of: Pakistan.

Indiana Montana Ohio Pennsylvania

Questions about this recall

Why was it recalled?

Elevating Monitor Suspension column dropping and will not rise back up.

Which lots are affected?

SKF Telescopic Pillar P/N ending in -003

Where was it sold?

Worldwide Distribution -US Distribution to states of: IN, OH, PA, and MT; and country of: Pakistan.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Omega Medical Imaging

All 4

Reported	Class	Recall	Company	Reason	Where
1 Nov 2023Device	CLASS II	Elevating Monitor Suspension Systems recalled by Omega Medical Imaging	Omega Medical Imaging	Other	11 states
1 Nov 2023Device	CLASS II	Elevating Monitor Suspension recalled by Omega Medical Imaging	Omega Medical Imaging	Other	Nationwide
14 Sep 2016Device	CLASS II	2 over 2 Elevating Monitor Suspension recalled by Omega Medical Imaging	Omega Medical Imaging	Other	14 states

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