# FDA enforcement report D-1289-2014

> FDA's dated enforcement report D-1289-2014 lists Class II and source status Terminated for AbbVie Inc. PeptideScanner connects the report to reviewed application NDA020263 through exact openFDA application-number annotations.

- Evidence object: `story:fda-enforcement-d-1289-2014:v1`
- Evidence domain: Safety
- Date in source: 2014-05-07
- Source checked: 2026-08-25
- Published by PeptideScanner: 2026-08-25
- Story landing page: https://peptidescanner.com/stories/fda-enforcement-d-1289-2014/
- JSON record: https://peptidescanner.com/evidence/v1/objects/fda-enforcement-d-1289-2014-v1.json
- Content SHA-256: `132dbc6e3ec3fd71a52e33a2ced5df56efdd9969dae010070aa945d44338aeb0`

## Claims and source pins

### Headline

FDA enforcement report D-1289-2014 ([`fda-enforcement-d-1289-2014-8c6d14481452`](#source-fda-enforcement-d-1289-2014-8c6d14481452))

### Summary

FDA's dated enforcement report D-1289-2014 lists Class II and source status Terminated for AbbVie Inc. PeptideScanner connects the report to reviewed application NDA020263 through exact openFDA application-number annotations. ([`fda-enforcement-d-1289-2014-8c6d14481452`](#source-fda-enforcement-d-1289-2014-8c6d14481452))

### Paragraph 1

FDA's dated enforcement report D-1289-2014 lists Class II and source status Terminated for AbbVie Inc. PeptideScanner connects the report to reviewed application NDA020263 through exact openFDA application-number annotations. ([`fda-enforcement-d-1289-2014-8c6d14481452`](#source-fda-enforcement-d-1289-2014-8c6d14481452))

### Paragraph 2

FDA's source-reported reason is: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with a potentially defective LuproLoc needle stick protection device. ([`fda-enforcement-d-1289-2014-8c6d14481452`](#source-fda-enforcement-d-1289-2014-8c6d14481452))

### Paragraph 3

This PeptideScanner lane is a bounded, dated FDA enforcement-report snapshot connected through an exact openFDA application-number annotation. It is not a medical alert or complete recall-lifecycle tracker, does not establish current product or recall status, does not identify affected lots, and does not provide medical guidance. ([`fda-enforcement-d-1289-2014-8c6d14481452`](#source-fda-enforcement-d-1289-2014-8c6d14481452))

## Sources

<a id="source-fda-enforcement-d-1289-2014-8c6d14481452"></a>
- **FDA enforcement report D-1289-2014 · Class II · report date 2014-05-07 · source status Terminated** — FDA enforcement reports via openFDA; class A. [Open source](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1289-2014%22&limit=1) (`fda-enforcement-d-1289-2014-8c6d14481452`)

## Correction lineage

No correction is recorded for this version.

## Reporting boundaries and unknowns

PeptideScanner reports the cited safety or enforcement record. It is not an individualized risk assessment or medical recommendation.

- Sources outside the selected public PeptideScanner bundle may exist and are not represented by this object.
- This object does not determine whether cited records agree, corroborate one another, or establish scientific truth.
- This object does not determine safety, efficacy, causality, or suitability for any person.

Methodology: https://peptidescanner.com/methodology/
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## Suggested citation

PeptideScanner. "FDA enforcement report D-1289-2014." Version 1, published 2026-08-25. https://peptidescanner.com/evidence/v1/objects/fda-enforcement-d-1289-2014-v1.json SHA-256: 132dbc6e3ec3fd71a52e33a2ced5df56efdd9969dae010070aa945d44338aeb0.