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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 65769

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

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Event summary

Timeline bucket
July 22, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
MCKESSON 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

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

Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product Usage: Automated anesthesia cart that monitors and controls the dispensing of medications, narcotics and supplies during surgical procedures.

Z-2089-2013
Recall number
Z-2089-2013
Initiated
July 22, 2013
Classification
Class II
Status
Terminated
Recalling firm
MCKESSON TECHNOLOGIES INC
Quantity
106

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.

Code information

Model Number (software version) 8.0.2 & 8.0.1 with RapiDispense

Distribution pattern

USA Nationwide Distribution in the states AR, MD, NJ, NY, PA, and WV.