# FDA recall D-579-2013

> **Petnet Solution Inc** · Class II · drug recall initiated 2013-02-22.

## Product

Fludeoxyglucose F 18 Injection USP, 20-200 mCi/mL, Diagnostic - For Intravenous Use Only, Manufactured by PETNET Solutions, Inc., Knoxville, TN

## Reason for recall

cGMP Deviation

## Distribution

Within the state of CA.

## Key facts

- **Recall number:** D-579-2013
- **Recalling firm:** Petnet Solution Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-02-22
- **Report date:** 2013-06-12
- **Termination date:** 2013-06-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Irvine, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-579-2013

## Citation

> AI Analytics. FDA recall D-579-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-579-2013. Source: US FDA. Licensed CC0.

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