Fort Defiance Industries recalls P213: Automated Field Steam Sterilizers with improper electrical grounding. Affected units may cause electric shock if mishandled.
The rear heater plate and cover assembly that contains the electrical wiring for the heaters does not have sufficient bonding to ground.
Fort Defiance Industries is recalling P2131 Automated Field Steam Sterilizers due to a potential electrical grounding issue. This could lead to electric shock if the device is mishandled or improperly installed.
The rear heater plate and cover assembly lacks sufficient bonding to ground the electrical wiring. This could cause electric shock if the device is mishandled or improperly installed, especially in environments with high moisture or electrical interference.
Users of the P2131 sterilizers, particularly those in medical or field settings where the device is used frequently. Individuals handling the equipment without proper grounding precautions are at higher risk.
Check for the model number P2131 and serial numbers AFS-0001 through AFS-0386 (excluding AFS-0297, which was not manufactured). The device is sold under the NSN 6530-01-641-4641.
Look for the serial numbers AFS-0001 through AFS-0386 on the device label.
If the device has a serial number in the affected range, stop using it immediately until a safe fix is implemented.
Check if your sterilizer has the model number P2131 and serial numbers AFS-0001 through AFS-0386 (excluding AFS-0297).
Stop using the device immediately and contact Fort Defiance Industries for further instructions.
The recall record does not specify a fix or remedy.
We’ve drafted a message you can send Fort Defiance to request your refund or repair — edit it as you like.
Subject: Recall Z-0121-2022 — Fort Defiance Fort Defiance Hello, I own a Fort Defiance that is covered by recall Z-0121-2022 from Fort Defiance. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.