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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 89414

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

Open FDA event record

Event summary

Timeline bucket
December 23, 2021
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Hill-Rom, Inc.

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

Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010

Z-0639-2022
Recall number
Z-0639-2022
Initiated
December 23, 2021
Classification
Class II
Status
Ongoing
Recalling firm
Hill-Rom, Inc.
Quantity
5470 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Missing bushing on Liko M220 and M230 causing wear and potential for patient falling

Code information

Serial numbers: 5263715-5269464. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Austria, Austria, Bahrain, Canada, Switzerland, Germany, Denmark, Spain, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Israel, Italy, Norway, Saudi Arabia, Sweden, Slovenia, Taiwan (Province of China), South Africa, Oman.

device · product 2 of 2

Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015

Z-0640-2022
Recall number
Z-0640-2022
Initiated
December 23, 2021
Classification
Class II
Status
Ongoing
Recalling firm
Hill-Rom, Inc.
Quantity
1215 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Missing bushing on Liko M220 and M230 causing wear and potential for patient falling

Code information

Serial numbers: 5361393-5362761. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Austria, Austria, Bahrain, Canada, Switzerland, Germany, Denmark, Spain, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Israel, Italy, Norway, Saudi Arabia, Sweden, Slovenia, Taiwan (Province of China), South Africa, Oman.