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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93581

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

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Event summary

Timeline bucket
December 06, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Abiomed, 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

Impella Connect, software portal for online device management that allows clinicians and Impella support staff to remotely view Impella data.

Z-0636-2024
Recall number
Z-0636-2024
Initiated
December 06, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Abiomed, Inc.
Quantity
n/a - no physical product

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The following features have been disabled from the web-based portal because the FDA has not evaluated these features for safety and effectiveness: Notifications via email feature; AIC alarm color on case tile feature; Sort case tiles by AIC alarm color feature; Pump metric display on case tile feature

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

No Marketing Application

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The following features have been disabled from the web-based portal because the FDA has not evaluated these features for safety and effectiveness: Notifications via email feature; AIC alarm color on case tile feature; Sort case tiles by AIC alarm color feature; Pump metric display on case tile feature

Code information

UDI-DI 00813502011647 Software version 1.1 - 3.17.1

Distribution pattern

Domestic distribution nationwide.

Field note

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