Drug recall
0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL…
FDA recall event 77824 · Class II · ICU Medical Inc
Key facts
| Event ID | 77824 |
|---|---|
| Recall numbers | D-1091-2017 |
| Recalling firm | ICU Medical Inc |
| Product type | Drugs |
| Products | 0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Presence of Particulate Matter; stainless steel |
| Initiation date | Jul 26, 2017 |
| Report date | Aug 23, 2017 |
| Termination date | Mar 11, 2019 |
| 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: