FDA Device recall Z-2983-2026
Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131
- FDA Device
- Class II
- ongoing
- Published 2026-08-26
On 2026-08-26 the FDA classified a Class II recall of Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131 by Fort Defiance Industries, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2983-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-08 |
| Published | 2026-08-26 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Fort Defiance Industries |
| Distribution | US |
Product
Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131
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.
Identifiers
| code_info | Lot Code: All serial numbers/ GTIN: (01) 00862992000327 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2983-2026%22
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