# FDA recall D-0547-2018

> **Fagron, Inc** · Class II · drug recall initiated 2018-02-14.

## Product

SyrSpend SF Suspending Base, a) 500 mL (NDC 51552-1079-5) and b) 4 L (NDC 51552-1079-9), Rx Only, Manufactured by Fagron Inc. St. Paul, MN 55120

## Reason for recall

Microbial contamination of Non-Sterile Product;  product contamination with yeast and mold (Paecilomyces saturatus and Aspergillus fumigatus).

## Distribution

Nationwide, USA

## Key facts

- **Recall number:** D-0547-2018
- **Recalling firm:** Fagron, Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-02-14
- **Report date:** 2018-03-07
- **Termination date:** 2019-09-10

- **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-0547-2018

## Citation

> AI Analytics. FDA recall D-0547-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0547-2018. Source: US FDA. Licensed CC0.

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