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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 80556

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

Open FDA event record

Event summary

Timeline bucket
November 03, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Handicare Usa 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

Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

Z-2752-2018
Recall number
Z-2752-2018
Initiated
November 03, 2017
Classification
Class II
Status
Terminated
Recalling firm
Handicare Usa Inc
Quantity
716

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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

Premature strap wear and breakage at maximum weight conditions (625 lbs.).

Code information

Device Model; 323100, 323102, 323117, 323118, 323120, 323137, 323149, 323150, 323215, 323225, 323237, 323240, 323400, 323417, 323450, 323600, 323602, 323700, 323750, 323840, 323851, 323917, 323117V, and 323150V

Distribution pattern

Worldwide Distribution - US Nationwide in the states of AK, CA, CT, DE, GA, IA, IL, KY, LA, MA, ME, MI, MN, MO, NE, NV, NY, OH, OR, PA, RI, TN, TX, WI, and Puerto Rico and the countries of Canada and Australia,

device · product 2 of 2

Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

Z-2753-2018
Recall number
Z-2753-2018
Initiated
November 03, 2017
Classification
Class II
Status
Terminated
Recalling firm
Handicare Usa Inc
Quantity
4

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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

Premature strap wear and breakage at maximum weight conditions (625 lbs.).

Code information

Device Model; 303090 and 303093

Distribution pattern

Worldwide Distribution - US Nationwide in the states of AK, CA, CT, DE, GA, IA, IL, KY, LA, MA, ME, MI, MN, MO, NE, NV, NY, OH, OR, PA, RI, TN, TX, WI, and Puerto Rico and the countries of Canada and Australia,