Class I — Fresenius Medical Care Holdings, Inc.
| Recalling firm | Fresenius Medical Care Holdings, Inc. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class I |
| Status | Ongoing |
| Reason | Potential PCBA leaching from tubing of hemodialysis machines. |
| Product | 2008T Hemodialysis SYS, with CDX |
| Quantity | 703 units |
| Distribution | Domestic: Nationwide Distribution. |
| Initiated | 2023-09-06 |
| Classified | 2023-10-06 |
| Recall number | Z-0028-2024 |
| 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 I recall — Fresenius Medical Care Holdings, Inc. (Z-0028-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/92788/
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