Drug recall
power cord for: (a) AMIA Automated PD Cycler, Product Code: 5C9320; (b) Kaguya PD System, Product Code…
FDA recall event 80522 · Class II · Baxter Healthcare Corporation
Key facts
| Event ID | 80522 |
|---|---|
| Recall numbers | Z-2597-2018 |
| Recalling firm | Baxter Healthcare Corporation |
| Product type | Devices |
| Products | power cord for: (a) AMIA Automated PD Cycler, Product Code: 5C9320; (b) Kaguya PD System, Product Code: T5C8500 (Japanese distribution only) |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | There were instances where the power cord socket detached from the back of the AMIA cycler when the power cord was unplugged from the socket. |
| Initiation date | Jul 12, 2018 |
| Report date | Aug 8, 2018 |
| Termination date | Mar 31, 2021 |
| 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: