Drug recall
Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131
FDA recall event 99371 · Class II · Fort Defiance Industries, LLC
Key facts
| Event ID | 99371 |
|---|---|
| Recall numbers | Z-2983-2026 |
| Recalling firm | Fort Defiance Industries, LLC |
| Product type | Devices |
| Products | Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Jul 8, 2026 |
| Report date | Aug 26, 2026 |
| City | Loudon |
| State | TN |
| Country | United States |
| FEI number | 3011421558 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: