Class II — Fort Defiance Industries, LLC
| Recalling firm | FORT DEFIANCE INDUSTRIES |
|---|---|
| Registered facility | FORT DEFIANCE INDUSTRIES LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which could result in an unreliable fault current return path. |
| Product | Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131 |
| Distribution | Worldwide - US Nationwide distribution in the states of MD, VA, NJ, TN and the countries of Canada, Lithuania, Spain. |
| Initiated | 2026-07-08 |
| Classified | 2026-08-18 |
| Recall number | Z-2983-2026 |
| 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 — Fort Defiance Industries, LLC (Z-2983-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99371/
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