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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 64512

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
February 15, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Moller Vital

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

Molift Smart 150

Z-1342-2013
Recall number
Z-1342-2013
Initiated
February 15, 2013
Classification
Class II
Status
Terminated
Recalling firm
Moller Vital
Quantity
7,555 units subject to review; US: 1,280 units - Foreign: 6,275 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.

Code information

Art #: 0920001 batch 1-62 and 0920002 batch 1-77; Serial Number ranges 022228 to 094103 and 100015 to 12058.

Distribution pattern

US Nationwide Distribution: CA, FL, GA, ID, IL, KY, MA, ME, MI, MN, NC, NH, NJ, NM, NV, NY, OH, OK, PA, TN, TX, VT, WA and Hawaii. Foreign Distribution:: Australia, Austria; Belgium, Denmark, Finland, France, Germany, Iceland, Israel, Italy, Japan, Netherlands, New Zealand, Norway, Spain, Sverige, Switzerland, United Kingdom.

device · product 2 of 2

Molift Smart 150

Z-1343-2013
Recall number
Z-1343-2013
Initiated
February 15, 2013
Classification
Class II
Status
Terminated
Recalling firm
Moller Vital
Quantity
Subject to recall 1,460 units; US: 175 units; Foreign: 1,285 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.

Code information

Art #: 0920008; Serial Number range 20941 to 27299.

Distribution pattern

US Nationwide Distribution: CA, FL, GA, ID, IL, KY, MA, ME, MI, MN, NC, NH, NJ, NM, NV, NY, OH, OK, PA, TN, TX, VT, WA and Hawaii. Foreign Distribution:: Australia, Austria; Belgium, Denmark, Finland, France, Germany, Iceland, Israel, Italy, Japan, Netherlands, New Zealand, Norway, Spain, Sverige, Switzerland, United Kingdom.