SyrSpend SF — Class II drug recall D-0655-2016
Terminated recall by Fagron, Inc, reported 2016-02-17, distributed nationwide. Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF Grape Flavor are being recalled d
| Recall number | D-0655-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fagron, Inc, Saint Paul, MN, United States |
| Recall initiated | 2015-11-11 |
| Classified | 2016-02-05 |
| Reported by FDA | 2016-02-17 |
| Terminated | 2017-08-22 |
| Distributed | Nationwide (US) |
| Quantity | 148 bottles |
| Reason classes | microbial contamination, sterility |
| Pathogens | yeast |
| NDC | 51552-1167-09 |
| Lot numbers | 15A05-U03-022765, 15A05-U06-023277, 15G29-U03-025975 |
Product
SyrSpend SF, Suspending Base, Grape Flavored, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 4 L bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1167-9.
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.
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-0655-2016. 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.