Drug recall
Budesonide BP Micronized, 500mg, 5g, 1g, 25g, 100g bottles, Caution: For manufacturing, processing and…
FDA recall event 26457 · Class II · Meridian Pharmaceuticals Inc.
Key facts
| Event ID | 26457 |
|---|---|
| Recall numbers | D-274-3 |
| Recalling firm | Meridian Pharmaceuticals Inc. |
| Product type | Drugs |
| Products | Budesonide BP Micronized, 500mg, 5g, 1g, 25g, 100g bottles, Caution: For manufacturing, processing and repackaging, Packaged by Meridian Pharmaceuticals, Inc., Decatur, AL 35601 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent |
| Initiation date | Jun 4, 2003 |
| City | Decatur |
| Country | United States |
| FEI number | 3003063918 |
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