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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 80465

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

Open FDA event record

Event summary

Timeline bucket
February 12, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Arjohuntleigh Magog

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

Quick Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with patient lifters to measure the weight of a patient who cannot stand on a scale. It is designed to be used indoors in hospitals, nursing homes, home care or health care facilities.

Z-2660-2018
Recall number
Z-2660-2018
Initiated
February 12, 2018
Classification
Class II
Status
Terminated
Recalling firm
Arjohuntleigh Magog
Quantity
874 Units (both styles)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The spreader bar can detach from the scale attachment under certain conditions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The spreader bar can detach from the scale attachment under certain conditions.

Code information

Product Code 700-19485: starting from serial number 300146551 up to serial number 300220716.

Distribution pattern

Worldwide distribution: US (nationwide) to states of: CO, FL, IA, IL, KY, MN, NY, PH, and WA; and countries of: Australia, Belgium, Brazil, Canada, China, France, Germany, Hong Kong, Ireland, Italy, Japan, Netherlands, Norway, Singapore, Swiss, Turkey, United Kingdom, and United Arab Emirates.

device · product 2 of 2

Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with patient lifters to measure the weight of a patient who cannot stand on a scale. It is designed to be used indoors in hospitals, nursing homes, home care or health care facilities.

Z-2661-2018
Recall number
Z-2661-2018
Initiated
February 12, 2018
Classification
Class II
Status
Terminated
Recalling firm
Arjohuntleigh Magog
Quantity
874 Units (both styles)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The spreader bar can detach from the scale attachment under certain conditions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The spreader bar can detach from the scale attachment under certain conditions.

Code information

Product Code 700-19490: starting from serial number 300142013 up to serial number 300219867.

Distribution pattern

Worldwide distribution: US (nationwide) to states of: CO, FL, IA, IL, KY, MN, NY, PH, and WA; and countries of: Australia, Belgium, Brazil, Canada, China, France, Germany, Hong Kong, Ireland, Italy, Japan, Netherlands, Norway, Singapore, Swiss, Turkey, United Kingdom, and United Arab Emirates.