# FDA recall D-0654-2016

> **Fagron, Inc** · Class II · drug recall initiated 2015-11-11.

## Product

SyrSpend SF, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 500 mL bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1079-5.

## Reason for recall

Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF Grape Flavor are being recalled due to the presence of yeast.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0654-2016
- **Recalling firm:** Fagron, Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-11-11
- **Report date:** 2016-02-17
- **Termination date:** 2017-08-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0654-2016

## Citation

> AI Analytics. FDA recall D-0654-2016. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0654-2016. Source: US FDA. Licensed CC0.

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