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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82178

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

Open FDA event record

Event summary

Timeline bucket
February 12, 2019
Product types
Device
Classifications
Class I
Statuses
Terminated
Recalling firm wording
O-Two Medical Technologies, Inc.

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

e500 Automatic Transport Ventilator, Model Number 01EVE500

Z-0976-2019
Recall number
Z-0976-2019
Initiated
February 12, 2019
Classification
Class I
Status
Terminated
Quantity
136

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main board causing the screw to rub against the bottom side of the board, wearing away the insulation layer and creating a short circuit.

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

There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main board causing the screw to rub against the bottom side of the board, wearing away the insulation layer and creating a short circuit.

Code information

EV50001 to EV50148

Distribution pattern

The products were distributed to the following US states: AZ, CA, CO, FL, OH, PA, TX, and VA.

device · product 2 of 3

e600 Automatic Transport Ventilator, Model Number 01EVE600

Z-0977-2019
Recall number
Z-0977-2019
Initiated
February 12, 2019
Classification
Class I
Status
Terminated
Quantity
119

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main board causing the screw to rub against the bottom side of the board, wearing away the insulation layer and creating a short circuit.

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

There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main board causing the screw to rub against the bottom side of the board, wearing away the insulation layer and creating a short circuit.

Code information

EV60001 to EV60126

Distribution pattern

The products were distributed to the following US states: AZ, CA, CO, FL, OH, PA, TX, and VA.

device · product 3 of 3

e700 Automatic Transport Ventilator, Model Number 01EVE700

Z-0978-2019
Recall number
Z-0978-2019
Initiated
February 12, 2019
Classification
Class I
Status
Terminated
Quantity
632

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main board causing the screw to rub against the bottom side of the board, wearing away the insulation layer and creating a short circuit.

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

There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main board causing the screw to rub against the bottom side of the board, wearing away the insulation layer and creating a short circuit.

Code information

EV70001 to EV70658

Distribution pattern

The products were distributed to the following US states: AZ, CA, CO, FL, OH, PA, TX, and VA.

Field note

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