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 rear heater plate and cover assembly that contains the electrical wiring for the heaters does not have sufficient bonding to ground. |
| Product | P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641 |
| Quantity | 380 devices |
| Distribution | Distributed nationwide to PA, MD, TX, NJ, OH, TN, UT, VA and internationally to Canada. |
| Initiated | 2021-08-19 |
| Classified | 2021-10-15 |
| Recall number | Z-0121-2022 |
| 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-0121-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88628/
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