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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96729

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

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Event summary

Timeline bucket
May 21, 2025
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Jolife 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

LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.

Z-1998-2025
Recall number
Z-1998-2025
Initiated
May 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Jolife AB
Quantity
5 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.

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

Due to demonstration units of chest compression system being provided to a customer which may potentially be utilized for clinical use.

Code information

Lucus 2 Catalog Number: 99576-000025 UDI-DI code: 00883873904565 Serial Number: 30090111 Lucas 3 Catalog Number: 21331-000081 UDI-DI code: 00883873861875 Serial Numbers: 35172335 35160570 Lucas 3.1 Catalog Number: 94576-000005 UDI-DI code: 00883873834329 Serial Numbers: 3518A164 3518D104 (Scrapped)

Distribution pattern

U.S. Nationwide distribution in the states of IN, MI, OH and TX.