Class II — Isopure Corp
| Recalling firm | ISOPURE CORP. |
|---|---|
| Registered facility | ISOPURE, CORP. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | There is a potential for an uneven plastic encapsulation of the magnet ring during the molding process and partial axial displacement. This issue could cause uneven wear during use, cause exposure of the magnet to solution, and thereby result in corrosion and the presence of iron. |
| Product | Finish Thompson Centrifugal Pump Model #110192-3 (sold as spare part) |
| Quantity | 8 |
| Distribution | The products were distributed to the following US states: AL, FL, GA, MA, MD, MN, NC, NM, NY, OH, OK, TX, and VA. |
| Initiated | 2019-04-19 |
| Classified | 2020-01-18 |
| Terminated | 2020-05-29 |
| Recall number | Z-0823-2020 |
| 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 — Isopure Corp (Z-0823-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83990/
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