Drug recall
Cromolyn Sodium Inhalation Solution USP 20 mg/2 mL Unit Dose Vials, 60 and 120 count boxes, Rx only, Steri-Neb…
FDA recall event 47399 · Class III · IVAX Pharmaceuticals
Key facts
| Event ID | 47399 |
|---|---|
| Recall numbers | D-182-2008 |
| Recalling firm | IVAX Pharmaceuticals |
| Product type | Drugs |
| Products | Cromolyn Sodium Inhalation Solution USP 20 mg/2 mL Unit Dose Vials, 60 and 120 count boxes, Rx only, Steri-Neb brand of Sterile Unit Dose Vials, Not For Injection Aqueous Solution for Nebulization… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed pH Specification |
| Initiation date | Mar 12, 2008 |
| Termination date | Apr 23, 2009 |
| City | Miami |
| State | FL |
| Country | United States |
| FEI number | 1000140211 |
At a glance
- 1–9 Products in this recall
- 1–9 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