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 | Terminated |
| Reason | During long-term storage (i.e. military depot), the interaction of stagnant water and dissimilar metals in the plumbing of the P2131 device produces deposits in the water system that can potentially interfere with the rear sight gauge and / or the water liquid level switch. |
| Product | FDI FORT DEFIANCE INDUSTRIES P2131 AUTOMATED FIELD STEAM STERILIZER, NSN: 6530-01-641-4641 Product Usage: The Fort Defiance Industries Automated Field Steam Sterilizer Model P2131 is designed for sterilization of porous and non-porous, heat- and moisture-stable materials (e.g., surgical instruments and textiles) used in healthcare facilities. The P2131 sterilizer is a transportable device designed for use in a variety of austere environments. |
| Quantity | 199 units |
| Distribution | US Nationwide Distribution in the states of PA. VA. TX |
| Initiated | 2018-05-24 |
| Classified | 2018-07-10 |
| Terminated | 2023-06-27 |
| Recall number | Z-2411-2018 |
| 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-2411-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80293/
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