Drug recall
Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible containers, Rx only, Hospira, Inc., Lake…
FDA recall event 63432 · Class I · Hospira Inc.
Key facts
| Event ID | 63432 |
|---|---|
| Recall numbers | D-263-2013 |
| Recalling firm | Hospira Inc. |
| Product type | Drugs |
| Products | Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible containers, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7929-09. |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Non-Sterility: One confirmed customer report that product contained spore-like particulates, consistent with mold. |
| Initiation date | Oct 5, 2012 |
| Report date | Apr 24, 2013 |
| Termination date | Aug 21, 2015 |
| City | Lake Forest |
| State | IL |
| Country | United States |
| FEI number | 3005579246 |
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: