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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 80911

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 17, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Liko AB

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

1 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 1

Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.

Z-0105-2019
Recall number
Z-0105-2019
Initiated
July 17, 2018
Classification
Class II
Status
Terminated
Recalling firm
Liko AB
Quantity
2

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products manufactured on 5/5/17 may be assembled incorrectly. If the incorrectly assembled products is used for patient transport, this could allow the patient to fall, resulting in potential injury to the patient.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Storage

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The products manufactured on 5/5/17 may be assembled incorrectly. If the incorrectly assembled products is used for patient transport, this could allow the patient to fall, resulting in potential injury to the patient.

Code information

Part Number 3136250, the manufacturing date is on the right side of the label listed as 2017-05-05.

Distribution pattern

The products were distributed to the following US states: OH.