FDAClass II · Medical device · Recall Z-2983-2026 · Recalled August 26, 2026

Fort Defiance Industries (FDI) recall — Fort Defiance Industries, LLC

Agency report date: August 26, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Fort Defiance Industries (FDI)
Company / brand: Fort Defiance Industries
Lot / serial / date codes: Lot Code: All serial numbers/ GTIN: (01) 00862992000327
Distribution: Worldwide - US Nationwide distribution in the states of MD, VA, NJ, TN and the countries of Canada, Lithuania, Spain.

Agency product description and boundaries

Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Fort Defiance Industries (FDI) recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2983-2026
Brand: All Fort Defiance Industries recalls
Classification: Class II
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Fort Defiance Industries (FDI) recall status

Companies & origin

Recalling firm location: Loudon, TN, United States
Firm address: 2411 Maremont Pkwy, 37774-1066

Identifying details (verbatim from the notice)

Product codes / lots: Lot Code: All serial numbers/ GTIN: (01) 00862992000327
Distribution: Worldwide - US Nationwide distribution in the states of MD, VA, NJ, TN and the countries of Canada, Lithuania, Spain.
FDA event ID: 99371
Recall initiated: July 8, 2026
FDA classified: August 18, 2026
FDA report date: August 26, 2026

Other medical device recalls from around the same time

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BMC/REACTHEALTH Luna G3 APAP REF LG 3600 recall — BMC Medical Co., Ltd.FDA · August 26, 2026
Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus recall — Boston Scientific CorporationFDA · August 26, 2026
Boston Scientific ENROUTE Transcarotid Neuroprotection System recall — Boston Scientific CorporationFDA · August 26, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved October 22, 2026 at 6:00 PM UTC.

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