SyrSpend SF Suspending Base — Class II drug recall D-0547-2018
Terminated recall by Fagron, Inc, reported 2018-03-07, distributed nationwide. Microbial contamination of Non-Sterile Product; product contamination with yeast and mold (Paecilomyces satura
| Recall number | D-0547-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fagron, Inc, Saint Paul, MN, United States |
| Recall initiated | 2018-02-14 |
| Classified | 2018-02-27 |
| Reported by FDA | 2018-03-07 |
| Terminated | 2019-09-10 |
| Distributed | Nationwide (US) |
| Reason classes | microbial contamination, sterility |
| Pathogens | mold, yeast |
| NDC | 51552-1079-05, 51552-1079-09 |
| Expiration dates | 2020-10-02 |
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).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0547-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.