Drug recall
Baxa Vial Adapter, 14mm - Luer Lock, Order No. REF: 90, Quantity: 50 each, Single Use. Product Code H93890…
FDA recall event 66082 · Class II · Baxa Corporation
Key facts
| Event ID | 66082 |
|---|---|
| Recall numbers | Z-2165-2013 |
| Recalling firm | Baxa Corporation |
| Product type | Devices |
| Products | Baxa Vial Adapter, 14mm - Luer Lock, Order No. REF: 90, Quantity: 50 each, Single Use. Product Code H93890. Used as a needleless access device for reconstitution and drug transfer. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Baxter Healthcare Corporation is voluntarily recalling one lot of Baxa Vial Adapters, 14mm - Luer Lock, due to incorrect expiry date. |
| Initiation date | Aug 22, 2013 |
| Report date | Sep 18, 2013 |
| Termination date | Aug 19, 2016 |
| City | Englewood |
| State | CO |
| Country | United States |
| FEI number | 1419106 |
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 · Source date: