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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79968

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

Open FDA event record

Event summary

Timeline bucket
May 04, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Randox Laboratories

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

RX Imola (RX4900) For Professional Use for the quantitative in vitro determination of various clinical chemistry tests.

Z-2059-2018
Recall number
Z-2059-2018
Initiated
May 04, 2018
Classification
Class II
Status
Terminated
Recalling firm
Randox Laboratories
Quantity
41 analyzers

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software could

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Abnormal premature termination of the software could affect the use of the analyser when running patient samples. The impact being a delay in reporting test results.

Code information

GTIN 05055273206104. All serial numbers.

Distribution pattern

US Distribution including Puerto Rico and the state of : West Virginia.