Drug recall
Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line injection…
FDA recall event 90730 · Class I · Baxter Healthcare Corporation
Key facts
| Event ID | 90730 |
|---|---|
| Recall numbers | Z-1653-2022 |
| Recalling firm | Baxter Healthcare Corporation |
| Product type | Devices |
| Products | Baxter CLEARLINK System, Non-DEHP Solution Set with DUO-VENT Spike, Product Code 2R8403. An in-line injection site. |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Firm noted an increase in customer reports of leaks. |
| Initiation date | Aug 9, 2022 |
| Report date | Sep 21, 2022 |
| Termination date | Aug 9, 2024 |
| City | Deerfield |
| State | IL |
| Country | United States |
| FEI number | 1417572 |
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: