Drug recall
Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing IV catheters and…
FDA recall event 80702 · Class II · Medline Industries Inc
Key facts
| Event ID | 80702 |
|---|---|
| Recall numbers | Z-2948-2018 |
| Recalling firm | Medline Industries Inc |
| Product type | Devices |
| Products | Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing IV catheters and IV tubing only. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Packaged with an incorrect overwrap. |
| Initiation date | Feb 1, 2018 |
| Report date | Sep 5, 2018 |
| Termination date | Oct 5, 2020 |
| City | Northfield |
| State | IL |
| Country | United States |
| FEI number | 1417592 |
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: