Drug recall
Naloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL Carpuject Single-use cartridge syringe…
FDA recall event 80167 · Class I · HOSPIRA INC, LAKE FOREST
Key facts
| Event ID | 80167 |
|---|---|
| Recall numbers | D-0906-2018 |
| Recalling firm | HOSPIRA INC, LAKE FOREST |
| Product type | Drugs |
| Products | Naloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL Carpuject Single-use cartridge syringe, Single unit (NDC 0409-1782-03) and 10 count box (NDC 0409-1782-69), Rx Only, Hospira Inc., Lake… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Presence of Particulate Matter; Potential for particulate matter on the syringe plunger. |
| Initiation date | Jun 4, 2018 |
| Report date | Jun 13, 2018 |
| Termination date | Mar 27, 2020 |
| City | LAKE FOREST |
| State | IL |
| Country | United States |
| FEI number | 3013422905 |
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: