Drug recall
BEVACIZUMAB 2.5 MG/0.1ML, pre-filled syringe (deliverable dose of 1.25MG in normject syringe) Repackaged by…
FDA recall event 81466 · Class II · Avella of Deer Valley, Inc. Store 38
Key facts
| Event ID | 81466 |
|---|---|
| Recall numbers | D-0224-2019 |
| Recalling firm | Avella of Deer Valley, Inc. Store 38 |
| Product type | Drugs |
| Products | BEVACIZUMAB 2.5 MG/0.1ML, pre-filled syringe (deliverable dose of 1.25MG in normject syringe) Repackaged by Avella Specialty Pharmacy, 24416 N 19th Avenue, Pheonix, AZ 85085. NDC 42852-001-24 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Lack of Assurance of Sterility |
| Initiation date | Oct 31, 2018 |
| Report date | Nov 14, 2018 |
| Termination date | Jan 18, 2019 |
| City | Phoenix |
| State | AZ |
| Country | United States |
| FEI number | 3012890460 |
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 · Source date: