Drug recall
0.9% Sodium Chloride Injection USP, 100 mL MINI-BAG Plus Container, Rx only, Baxter Healthcare Corporation…
FDA recall event 69962 · Class I · Baxter Healthcare Corp
Key facts
| Event ID | 69962 |
|---|---|
| Recall numbers | D-481-2015 |
| Recalling firm | Baxter Healthcare Corp |
| Product type | Drugs |
| Products | 0.9% Sodium Chloride Injection USP, 100 mL MINI-BAG Plus Container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, Product Code 2B0043, NDC 0338-0553-18. |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Presence of Particulate Matter: Confirmed customer complaints received for the presence of blue plastic, identified as fragments of the frangible from the vial adapter. |
| Initiation date | Dec 4, 2014 |
| Report date | Apr 15, 2015 |
| Termination date | Apr 14, 2017 |
| City | Deerfield |
| State | IL |
| Country | United States |
| FEI number | 1000539281 |
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: