# FDA recall D-0833-2016

> **AbbVie Inc.** · Class III · drug recall initiated 2016-03-24.

## Product

Zemplar (paricalcitol) capsules, 1 mcg, 30-count bottle, Rx Only, Mfd for AbbVie Inc. North Chicago, IL 60064, NDC 0074-4317-30.

## Reason for recall

Failed Content Uniformity Specifications

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0833-2016
- **Recalling firm:** AbbVie Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-03-24
- **Report date:** 2016-04-27
- **Termination date:** 2016-10-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** North Chicago, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0833-2016

## Citation

> AI Analytics. FDA recall D-0833-2016. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-0833-2016. Source: US FDA. Licensed CC0.

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