Drug recall
SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L…
FDA recall event 89805 · Class I · Fagron, Inc
Key facts
| Event ID | 89805 |
|---|---|
| Recall numbers | D-0856-2022 |
| Recalling firm | Fagron, Inc |
| Product type | Drugs |
| Products | 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. |
| Classification | Class I |
| Status | Completed |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli. |
| Initiation date | Mar 4, 2022 |
| Report date | May 18, 2022 |
| City | Saint Paul |
| State | MN |
| Country | United States |
| FEI number | 1000174332 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: