# FDA recall D-0972-2015

> **Hospira Inc.** · Class II · drug recall initiated 2015-04-13.

## Product

Ketorolac Tromethamine Inj. USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose vial, Rx Only, Hospira Inc., Lake Forest, IL --- NDC 00409-3795-01--- Also labeled under NOVAPLUS label NDC 00409-3795-49

## Reason for recall

Crystallization

## Distribution

Nationwide, Puerto Rico and Guam.

## Key facts

- **Recall number:** D-0972-2015
- **Recalling firm:** Hospira Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-04-13
- **Report date:** 2015-05-06
- **Termination date:** 2017-12-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lake Forest, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0972-2015

## Citation

> AI Analytics. FDA recall D-0972-2015. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/D-0972-2015. Source: US FDA. Licensed CC0.

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