# FDA recall D-0873-2016

> **Sanofi-Aventis U.S. LLC** · Class I · drug recall initiated 2015-10-28.

## Product

Auvi-Q (epinephrine injection, USP) Auto-Injector, 0.15 mg (a) 2 prefilled auto injectors + 1 trainer (NDC 0024-5831-02) and (b) 1 prefilled auto injector + 1 trainer (NDC 0024-5831-00), Rx Only, Manufactured for Sanofi-Aventis US, LLC Bridgewater, NJ  08807 A Sanofi Company

## Reason for recall

Defective Delivery System; potential to have inaccurate dosage delivery

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0873-2016
- **Recalling firm:** Sanofi-Aventis U.S. LLC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-10-28
- **Report date:** 2016-06-01
- **Termination date:** 2025-07-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bridgewater, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0873-2016

## Citation

> AI Analytics. FDA recall D-0873-2016. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0873-2016. Source: US FDA. Licensed CC0.

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