Drug recall
Phospholine Iodide (echothiophate iodide for opthalmic solution), 0.125%, 6.25mg/5 ml, Rx only, The package…
FDA recall event 45848 · Class II · Wyeth Ayerst Laboratories
Key facts
| Event ID | 45848 |
|---|---|
| Recall numbers | D-074-2008 |
| Recalling firm | Wyeth Ayerst Laboratories |
| Product type | Drugs |
| Products | Phospholine Iodide (echothiophate iodide for opthalmic solution), 0.125%, 6.25mg/5 ml, Rx only, The package contains 1 bottle of sterile echothiophate iodide for ophthalmic solution with 40 mg… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Lack of assurance of sterility; eye droppers were not subjected to radiation sterilization |
| Initiation date | Nov 9, 2007 |
| Termination date | Apr 28, 2009 |
| City | Philadelphia |
| State | PA |
| Country | United States |
| FEI number | 3000306541 |
At a glance
- 1–9 Products in this recall
- None 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