# FDA recall D-0145-2017

> **Sandoz Inc** · Class III · drug recall initiated 2016-10-19.

## Product

Ceftriaxone for Injection, USP, 1 gram, 10 Single use Vials, Rx only, For IM or I.V. Use, Manufactured by: Sandoz GMbH for Hospira Worldwide, Inc., Lake Forest, Il 60045, USA, Made in Austria,  NDC 0409-7332-01

## Reason for recall

Labeling: Missing Label

## Distribution

WI

## Key facts

- **Recall number:** D-0145-2017
- **Recalling firm:** Sandoz Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-10-19
- **Report date:** 2016-11-30
- **Termination date:** 2017-07-27

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0145-2017

## Citation

> AI Analytics. FDA recall D-0145-2017. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0145-2017. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*