FDA recall record

Savaria Concord Lifts Omega Incline Platform Lift recall — FDA Z-1880-2017

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…

Class IIclassification
Z-1880-2017official record ID
May 3, 2017report date

Recall record at a glance

Official recordZ-1880-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSavaria Concord Lifts, Inc.
Report dateMay 3, 2017
Recall initiation dateApr 12, 2017
Quantity74
LocationBrampton, N/A, Canada

Official product description

Omega Incline Platform Lift

Why the product was 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

Distribution information

Worldwide Distribution - US Distribution and to North America.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

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About this record

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