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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82241

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

Open FDA event record

Event summary

Timeline bucket
February 06, 2019
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Advanced Bionics, LLC

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

3 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 3

Na¿da CL Q30 Sound Processor, Sand Beige, Model Cl-5260-120; Silver Gray, Model Cl-5260-140; and Velvet Black, Model Cl-5260-150.

Z-1083-2019
Recall number
Z-1083-2019
Initiated
February 06, 2019
Classification
Class II
Status
Terminated
Recalling firm
Advanced Bionics, LLC
Quantity
4 sound processors

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
incorrect firmware

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The sound processors were loaded with the incorrect firmware.

Code information

Model Cl-5260-120 - Serial number 1047584, UDI (01)07630016838057(11)180309(21)1045784; Model Cl-5260-140 - Serial number 1047481, UDI (01)07630016829710(11)151208(21)1047481; and Serial number 1047482, UDI (01)07630016829710(11)151208(21)1047482; and Model Cl-5260-150 - Serial number 1082276, UDI (01)07630016838071(11)180925(21)1082276.

Distribution pattern

Distribution was made to NC. Foreign distribution was made to Canada, Argentina, Germany, South Africa, Egypt, Kuwait, and Iran. There was no government/military distribution.

device · product 2 of 3

Na¿da CI Q70 Sound Processor, Sand Beige, Model Cl-5245-120; Silver Gray, Model Cl-5245-140; and Velvet Black, Model Cl-5245-150.

Z-1084-2019
Recall number
Z-1084-2019
Initiated
February 06, 2019
Classification
Class II
Status
Terminated
Recalling firm
Advanced Bionics, LLC
Quantity
3 sound processors

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
incorrect firmware

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The sound processors were loaded with the incorrect firmware.

Code information

Model Cl-5245-120 - Serial number 1042838, UDI (01)07630016837814(11)150729(21)1042838; Model Cl-5245-140 - Serial number 1013129, UDI (01)07630016838262(11)181030(21)1013129; and Model Cl-5245-150 - Serial number 1033132, UDI (01)07630016838279(11)170525(21)1033132.

Distribution pattern

Distribution was made to NC. Foreign distribution was made to Canada, Argentina, Germany, South Africa, Egypt, Kuwait, and Iran. There was no government/military distribution.

device · product 3 of 3

Na¿da CI Q90 Sound Processor, Silver Gray, Model Cl-5280-140.

Z-1085-2019
Recall number
Z-1085-2019
Initiated
February 06, 2019
Classification
Class II
Status
Terminated
Recalling firm
Advanced Bionics, LLC
Quantity
1 sound processor

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
incorrect firmware

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The sound processors were loaded with the incorrect firmware.

Code information

Serial number 1066444, UDI (01)07630016838118(11)180725(21)1066444.

Distribution pattern

Distribution was made to NC. Foreign distribution was made to Canada, Argentina, Germany, South Africa, Egypt, Kuwait, and Iran. There was no government/military distribution.