SyrSpend SF Suspending Base — Class I drug recall D-0856-2022
Completed recall by Fagron, Inc, reported 2022-05-18, distributed nationwide. Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli.
| Recall number | D-0856-2022 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fagron, Inc, Saint Paul, MN, United States |
| Recall initiated | 2022-03-04 |
| Classified | 2022-05-09 |
| Reported by FDA | 2022-05-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, FR |
| Reason classes | microbial contamination, sterility |
| Pathogens | burkholderia |
| NDC | 51552-1123-05, 51552-1123-09 |
| Lot numbers | A67186 |
| Expiration dates | 2024-08-31 |
Product
SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx Only, Manufactured for Fagron, Inc., St. Paul, MN 55120.
Reason for recall
Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli.
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-0856-2022. 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.