Drug recall
Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx Only, Distributed by…
FDA recall event 93693 · Class I · PFIZER
Key facts
| Event ID | 93693 |
|---|---|
| Recall numbers | D-0261-2024 |
| Recalling firm | PFIZER |
| Product type | Drugs |
| Products | Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx Only, Distributed by: Hospira, Inc., Lake Forest, IL 68045, NDC 61703-332-18 |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Presence of particulate matter: glass |
| Initiation date | Dec 21, 2023 |
| Report date | Jan 31, 2024 |
| City | New York |
| State | NY |
| Country | United States |
| FEI number | 3027194079 |
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 · Source date: