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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 67490

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

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Event summary

Timeline bucket
February 06, 2014
Product types
Device
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Medtronic Vascular

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

Medtronic Everest 20cc Inflation Device; Model Number and Catalog Number: AC2205P The Everest 20cc Inflation device is designed to be used to inflate / deflate balloon catheters as well as to monitor pressure within the balloon. The Everest 20atm Device is outfitted with a manometer with measuring pressures ranging from vacuum to 20bars in 0.5 bar increments. The Everest 30atm Device is outfitted with a manometer with measuring pressures ranging from vacuum to 30bars in 0.5 bar increments. The manometers are accurate to within +/- 3% of the gauges full scale. The device is a sterile, single use device and is not implanted; it also does not come in direct contact with the patient. This product is packaged in an inner and outer Tyvek /poly layer pouch.

Z-1121-2014
Recall number
Z-1121-2014
Initiated
February 06, 2014
Classification
Class III
Status
Terminated
Recalling firm
Medtronic Vascular
Quantity
191 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Incorrect master label.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect master label.

Code information

Lot Number: 50755851

Distribution pattern

Nationwide Distribution including TX, ME, IA, PA, OR, and NH.