Drug recall
Ultane¿ (sevoflurane) Inhalation Anesthetic, 250mL bottles, Rx only, Manufactured for ABBOTT LABORATORIES…
FDA recall event 34571 · Class II · ABBOTT Labs
Key facts
| Event ID | 34571 |
|---|---|
| Recall numbers | D-194-6 |
| Recalling firm | ABBOTT Labs |
| Product type | Drugs |
| Products | Ultane¿ (sevoflurane) Inhalation Anesthetic, 250mL bottles, Rx only, Manufactured for ABBOTT LABORATORIES, North Chicago, IL, 60069, USA * Under license from Marusishi Pharmaceutical Co., LTD, 2-3-5… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Defective container; bottles may have pinholes which could cause product to leak or evaporate |
| Initiation date | Feb 9, 2006 |
| Termination date | Mar 7, 2008 |
| City | North Chicago |
| State | IL |
| Country | United States |
| FEI number | 3001630466 |
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