# FDA recall D-0865-2016

> **Hospira Inc.** · Class I · drug recall initiated 2016-03-18.

## Product

8.4% Sodium Bicarbonate Injection, USP 50mEq (1mEq/mL), 4.2 grams (84 mg/mL), 50 mL, Rx only, Hospira Inc, Lake Forest, IL 60045, NDC 0409-6625-02

## Reason for recall

Presence of Particulate Matter:  particulate matter identified as an insect in one vial.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0865-2016
- **Recalling firm:** Hospira Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2016-03-18
- **Report date:** 2016-06-01

- **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-0865-2016

## Citation

> AI Analytics. FDA recall D-0865-2016. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-0865-2016. Source: US FDA. Licensed CC0.

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