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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 61853

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

Open FDA event record

Event summary

Timeline bucket
April 26, 2012
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
MicroAire Surgical Instruments, LLC

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

Lipofilter 3000, model ASP-CAN-2, labeled in part ***MicroAire, 1641 Edlich Drive, Charlottesville, VA 22911, USA*** Product Usage: A fat collection canister intended for use during liposuction procedures.

Z-1792-2012
Recall number
Z-1792-2012
Initiated
April 26, 2012
Classification
Class II
Status
Terminated
Quantity
15 devices

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Medical device was not manufactured under Good Manufacturing Procedures and a user may be unable to sterilize the device according to procedures.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Component change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Medical device was not manufactured under Good Manufacturing Procedures and a user may be unable to sterilize the device according to procedures.

Code information

Lot Number: 0312200152

Distribution pattern

US Nationwide Distribution including the states of CA, OH and NY.