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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 69132

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

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Event summary

Timeline bucket
August 15, 2014
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Apollo Endosurgery 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

LAP-BAND AP SYSTEM AP Large with Access Port, Allergan, LAP-BAND AP SYSTEM Access Port I. Product was distributed for both the AP Large and AP Standard sizes. The LAP-BAND System is indicated for weight reduction for patients with obesity, with a Body Mass Index (BMI) of at least 40 kg/m2 or a BMI of at least 30 kg/m2 with one or more obesity related comorbid conditions.

Z-2732-2014
Recall number
Z-2732-2014
Initiated
August 15, 2014
Classification
Class II
Status
Terminated
Recalling firm
Apollo Endosurgery Inc
Quantity
10

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product was distributed past its expiration date.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software Manufacturing/Software Deployment

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Product was distributed past its expiration date.

Code information

Lap-Band System AP Standard Catalog Number B-2240; Serial Numbers: 17760203, 17704664, 17704665, 17760205, 17760179, 17704672, 17704667, 17704659, 17760194, 17704653

Distribution pattern

Distributed in the states of California, Delaware, Indiana, Missouri, New Jersey, New York, and Oregon.

Field note

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