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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 97354

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

Open FDA event record

Event summary

Timeline bucket
July 10, 2025
Product types
Device
Classifications
Class I
Statuses
Ongoing
Recalling firm wording
mo-Vis BVBA

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

6 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 6

Micro Joystick R-net. Electrical wheelchair component.

Z-2454-2025
Recall number
Z-2454-2025
Initiated
July 10, 2025
Classification
Class I
Status
Ongoing
Recalling firm
mo-Vis BVBA
Quantity
3 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.

Code information

Model No. P002-52; UDI-DI: 05407008320027; Serial No. 1000 to 1690.

Distribution pattern

US Nationwide distribution in the state of TX.

device · product 2 of 6

Multi Joystick R-net. Electrical wheelchair component.

Z-2455-2025
Recall number
Z-2455-2025
Initiated
July 10, 2025
Classification
Class I
Status
Ongoing
Recalling firm
mo-Vis BVBA
Quantity
3 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.

Code information

Model No. P002-62; UDI-DI: 05407008320041; Serial No. 1000 to 1690.

Distribution pattern

US Nationwide distribution in the state of TX.

device · product 3 of 6

IDM-MICRO-R. Electrical wheelchair component.

Z-2456-2025
Recall number
Z-2456-2025
Initiated
July 10, 2025
Classification
Class I
Status
Ongoing
Recalling firm
mo-Vis BVBA
Quantity
15 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.

Code information

Model No. PRSPS0014; UDI-DI: 05407008320836; Serial No. 1000 to 1690.

Distribution pattern

US Nationwide distribution in the state of TX.

device · product 4 of 6

IDM-MULTI-R. Electrical wheelchair component.

Z-2457-2025
Recall number
Z-2457-2025
Initiated
July 10, 2025
Classification
Class I
Status
Ongoing
Recalling firm
mo-Vis BVBA
Quantity
15 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.

Code information

Model No. PRSPS0016; UDI-DI: 05407008320850; Serial No. 1000 to 1690.

Distribution pattern

US Nationwide distribution in the state of TX.

device · product 5 of 6

All-round Joystick R-net Light. Electrical wheelchair component.

Z-2458-2025
Recall number
Z-2458-2025
Initiated
July 10, 2025
Classification
Class I
Status
Ongoing
Recalling firm
mo-Vis BVBA
Quantity
3 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.

Code information

Model No. P002-76; UDI-DI: 05407008320096; Serial No. 1000 to 2647.

Distribution pattern

US Nationwide distribution in the state of TX.

device · product 6 of 6

IDM-ARLITE-R. Electrical wheelchair component.

Z-2459-2025
Recall number
Z-2459-2025
Initiated
July 10, 2025
Classification
Class I
Status
Ongoing
Recalling firm
mo-Vis BVBA
Quantity
25 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.

Code information

Model No. PRSPS00018. UDI-DI: 05407008320102; Serial No. 1000 to 2647.

Distribution pattern

US Nationwide distribution in the state of TX.