LAP-BAND AP SYSTEM AP Large with Access Port — Class II medical device recall Z-2732-2014
Terminated recall by Apollo Endosurgery Inc, reported 2014-10-08, distributed in CA, DE, IN, MO, NJ, NY, OR. Product was distributed past its expiration date.
| Recall number | Z-2732-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Apollo Endosurgery Inc, West Lake Hills, TX, United States |
| Recall initiated | 2014-08-15 |
| Classified | 2014-09-30 |
| Reported by FDA | 2014-10-08 |
| Terminated | 2016-02-01 |
| Distributed | CA, DE, IN, MO, NJ, NY, OR |
| Quantity | 10 |
| Serial numbers | 17704653, 17704659, 17704664, 17704665, 17704667, 17704672, 17760179, 17760194, 17760203, 17760205 |
| Model numbers | B-2240 |
Product
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.
Reason for recall
Product was distributed past its expiration date.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2732-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.