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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 84828

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

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Event summary

Timeline bucket
January 28, 2020
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Breas Medical, 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

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

Protective Cover Vivo 55/65 (Used for Vivo 50/65), Part No. 006344. It is an accessory (i.e. protective cover) for the Vivo 50 and Vivo 65 ventilators - Product Usage: The protective cover is intended for additional protection of the Vivo 50, Vivo 55, Vivo 60 and Vivo 65 ventilators during transportation, and in hospital, institutional, and home care environments. It can be used while the Vivo ventilators is operating, for example mounted on a wheelchair, in a personal vehicle, or carried by hand. The device is not to be used with the protective cover while positioned in a warm place, such as in direct sunlight or close to a radiator. The protective cover includes the following features: transparent window for accessing front panel and buttons; port for patient circuit, cables, O2 inlet, and standby button; cooling air inlet; patient air inlet; straps for safe mounting; and cooling air outlet.

Z-1352-2020
Recall number
Z-1352-2020
Initiated
January 28, 2020
Classification
Class II
Status
Terminated
Recalling firm
Breas Medical, Inc.
Quantity
629

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The outlet hole of the exhalation valve control pressure tube on the ventilator may become obstructed by the protective cover.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

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Inspect official wording and provenance

Reason for recall

The outlet hole of the exhalation valve control pressure tube on the ventilator may become obstructed by the protective cover.

Code information

The cover does not have a lot number; these covers were distributed between 01/11/2018 and 12/17/2019

Distribution pattern

Worldwide distribution - US Nationwide distribution in the states of AR, CA, FL, GA, IA, IL, KS, MA, MI, MO, NJ, NY, OH, PR, SC, TX, VA, WI and countries distribution worldwide.

Field note

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