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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79676

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

Open FDA event record

Event summary

Timeline bucket
February 22, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Roche Diagnostics Corporation

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

4 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 4

cobas b 221<2>Roche OMNI S2 system catalog numbers: 3337111001 and 3337111692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit, glucose, lactate, urea/BUN, total hemoglobin, oxygen saturation, oxyhemoglobin, deoxyhemoglobin, carboxyhemoglobin, and methemoglobin in samples of whole blood, serum, plasma, and aqueous solutions as appropriate.

Z-1610-2018
Recall number
Z-1610-2018
Initiated
February 22, 2018
Classification
Class II
Status
Terminated
Quantity
1026 total products

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software responsible for starting scheduled AutoQC measurements (scheduler) will

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The software responsible for starting scheduled AutoQC measurements (scheduler) will not activate.

Code information

3337111001 and 3337111692 UDI: 04015630018307

Distribution pattern

USA ( nationwide)

device · product 2 of 4

Cobas b 221<4>Roche OMNI S4 system; Catalog numbers: 3337138001 and 3337138692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit, glucose, lactate, urea/BUN, total hemoglobin, oxygen saturation, oxyhemoglobin, deoxyhemoglobin, carboxyhemoglobin, and methemoglobin in samples of whole blood, serum, plasma, and aqueous solutions as appropriate.

Z-1611-2018
Recall number
Z-1611-2018
Initiated
February 22, 2018
Classification
Class II
Status
Terminated
Quantity
1026 total products

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software responsible for starting scheduled AutoQC measurements (scheduler) will

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The software responsible for starting scheduled AutoQC measurements (scheduler) will not activate.

Code information

Catalog numbers: 3337138001 and 3337138692 UDI: 04015630018321

Distribution pattern

USA ( nationwide)

device · product 3 of 4

cobas b 221<6>Roche OMNI S6 system; Catalog numbers: 3337154001 and 3337154692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit, glucose, lactate, urea/BUN, total hemoglobin, oxygen saturation, oxyhemoglobin, deoxyhemoglobin, carboxyhemoglobin, and methemoglobin in samples of whole blood, serum, plasma, and aqueous solutions as appropriate.

Z-1612-2018
Recall number
Z-1612-2018
Initiated
February 22, 2018
Classification
Class II
Status
Terminated
Quantity
1026 total products

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software responsible for starting scheduled AutoQC measurements (scheduler) will

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The software responsible for starting scheduled AutoQC measurements (scheduler) will not activate.

Code information

Catalog numbers: 3337154001 and 3337154692 UDI: 04015630018345

Distribution pattern

USA ( nationwide)

device · product 4 of 4

cobas b 221 AutoQC Module Complete; Catalog numbers: 3313522001 and 3313522692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit, glucose, lactate, urea/BUN, total hemoglobin, oxygen saturation, oxyhemoglobin, deoxyhemoglobin, carboxyhemoglobin, and methemoglobin in samples of whole blood, serum, plasma, and aqueous solutions as appropriate.

Z-1613-2018
Recall number
Z-1613-2018
Initiated
February 22, 2018
Classification
Class II
Status
Terminated
Quantity
1026 total products

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software responsible for starting scheduled AutoQC measurements (scheduler) will

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The software responsible for starting scheduled AutoQC measurements (scheduler) will not activate.

Code information

Catalog numbers: 3313522001 and 3313522692

Distribution pattern

USA ( nationwide)

Field note

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