Class II — Baxter Healthcare Corporation
| Recalling firm | BAXTER HEALTHCARE CORPORATION |
|---|---|
| Registered facility | View this company's 32 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential for no-flow and leaks under the twist clamp. |
| Product | MiniCap Extended Life PD Transfer Set |
| Quantity | 72,771 units |
| Distribution | Worldwide and US (Nationwide), Canada, Brazil, Mexico, Bermuda, and Indonesia |
| Initiated | 2020-11-10 |
| Classified | 2021-01-04 |
| Terminated | 2023-03-24 |
| Recall number | Z-0768-2021 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Baxter Healthcare Corporation (Z-0768-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/86883/
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