Drug recall
0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045…
FDA recall event 82048 · Class II · ICU Medical Inc
Key facts
| Event ID | 82048 |
|---|---|
| Recall numbers | D-0509-2019 |
| Recalling firm | ICU Medical Inc |
| Product type | Drugs |
| Products | 0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-09 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | CGMP Deviations |
| Initiation date | Feb 4, 2019 |
| Report date | Feb 27, 2019 |
| Termination date | Jun 4, 2020 |
| City | LAKE FOREST |
| State | IL |
| Country | United States |
| FEI number | 3013319212 |
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: