# FDA recall D-0976-2015

> **Hospira Inc.** · Class I · drug recall initiated 2015-03-05.

## Product

0.9% Sodium Chloride Injection, USP, 250 mL,  Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.

## Reason for recall

Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.

## Distribution

Nationwide.

## Key facts

- **Recall number:** D-0976-2015
- **Recalling firm:** Hospira Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-03-05
- **Report date:** 2015-05-13
- **Termination date:** 2016-06-09

- **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-0976-2015

## Citation

> AI Analytics. FDA recall D-0976-2015. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/D-0976-2015. Source: US FDA. Licensed CC0.

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