Drug recall
HICON(tm), Sodium Iodide I-131 solution USP, 1000 mCi fill size, Product #502880, Manufactured by: DRAXIMAGE…
FDA recall event 58106 · Class III · Draxis Specialty Pharmaceutical Inc.
Key facts
| Event ID | 58106 |
|---|---|
| Recall numbers | D-500-2011 |
| Recalling firm | Draxis Specialty Pharmaceutical Inc. |
| Product type | Drugs |
| Products | HICON(tm), Sodium Iodide I-131 solution USP, 1000 mCi fill size, Product #502880, Manufactured by: DRAXIMAGE, a Div. of DRAXIS Specialty Pharmaceuticals Inc., Kirkland, Quebec, Canada |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect expiration date |
| Initiation date | Feb 10, 2011 |
| Termination date | May 19, 2011 |
| City | Kirkland |
| Country | Canada |
| FEI number | 3001623073 |
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