CLASS II Device recall · Reported 3 May 2017 · FDA Enforcement Report

Omega Incline Platform Lift recalled by Savaria Concord Lifts

Savaria Concord Lifts is recalling Omega Incline Platform Lift. The recall was initiated on 12 Apr 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codess/n or lot number - Job Number 630046 through 630119

Quantity recalled74

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-1880-2017
FDA event ID: 77053
Recalling firm: Savaria Concord Lifts, Brampton, N/A
Classification: Class II
Status: Terminated
Recall initiated: 12 Apr 2017
FDA classified: 26 Apr 2017
Reported: 3 May 2017
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

12 Apr 2017	Recall initiated by company
26 Apr 2017	Classified by FDA	+14 days
3 May 2017	Published in enforcement report	+7 days

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

Reason for recall

Savaria Concord Lifts Inc has decided to initiate this recall of its Omega Incline Platform Lift because bolts can come loose causing the carriage to separate from the trolley and the unit to fail

Product as listed by the FDA

Omega Incline Platform Lift

Where it was distributed

Worldwide Distribution - US Distribution and to North America.

Questions about this recall

Why was it recalled?

Savaria Concord Lifts Inc has decided to initiate this recall of its Omega Incline Platform Lift because bolts can come loose causing the carriage to separate from the trolley and the unit to fail

Which lots are affected?

s/n or lot number - Job Number 630046 through 630119

Where was it sold?

Worldwide Distribution - US Distribution and to North America.

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.

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