Loudon, TN, United States
Fort Defiance Industries, LLC recalls
3 recalls recorded since 2018, most recently on 8 July 2026. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls3
Ongoing (FDA)2
Terminated or completed1
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 8 July 2026
- 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.
- Distribution
- Worldwide - US Nationwide distribution in the states of MD, VA, NJ, TN and the countries of Canada, Lithuania, Spain.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2983-2026
- Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131
Ongoing Class II Medical devices
- Recall started
- 19 August 2021
- Reason
- The rear heater plate and cover assembly that contains the electrical wiring for the heaters does not have sufficient bonding to ground.
- Distribution
- Distributed nationwide to PA, MD, TX, NJ, OH, TN, UT, VA and internationally to Canada.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0121-2022
- P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641
Terminated Class II Medical devices
- Recall started
- 24 May 2018
- Terminated
- 27 June 2023
- 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.
- Distribution
- US Nationwide Distribution in the states of PA. VA. TX
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2411-2018
- 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 por
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.