Class II — Xodus Medical Inc
| Recalling firm | XODUS MEDICAL, INC. |
|---|---|
| Registered facility | XODUS MEDICAL, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The sterile barrier of some devices may have been affected |
| Product | Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory |
| Quantity | 255,000 each |
| Distribution | Worldwide Distribution - US Nationwide in the States of : CA, ID, IL, LA, MD, NY, OH, OK, TX, VA, WI and OUS: Malaysia, Kuwait, Australia, Canada, UAE, Ireland, Korea, Saudi Arabia, Japan, Mexico |
| Initiated | 2019-09-19 |
| Classified | 2019-10-16 |
| Terminated | 2024-03-04 |
| Recall number | Z-0151-2020 |
| 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 — Xodus Medical Inc (Z-0151-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83819/
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