Steris recalls Dual Flat Panel Monitor accessories for HarmonyAIR E-Series surgical lighting systems due to potential yoke assembly detachment. Affected units have specific serial numbers.
The DFPM yoke assembly ("yoke assembly") may detach from the spring arm. Should the yoke assembly detach from the spring arm, the yoke assembly would not be expected to fully detach but rather hang from the wiring within the yoke assembly.
Steris is recalling certain Dual Flat Panel Monitor accessories for HarmonyAIR E-Series surgical lighting systems because the yoke assembly might detach from the spring arm. This could cause the yoke to hang from the wiring, potentially leading to interference with surgical procedures.
The yoke assembly may detach from the spring arm but won't fully separate. Instead, it hangs from the wiring inside the yoke, which could interfere with surgical procedures by obstructing the lighting system or causing unintended movements.
Surgical teams using the HarmonyAIR E-Series lighting systems with the recalled accessories are most at risk. The recall affects specific units identified by serial numbers.
Check if your HarmonyAIR E-Series surgical lighting system has a Dual Flat Panel Monitor accessory with the listed serial numbers. The recall includes specific units identified by their unique serial numbers.
Identify if your accessory has one of the listed serial numbers: 0416920048, 0417820084, 0417820088, and other specific numbers.
The yoke assembly may detach from the spring arm but won't fully separate; it hangs from the wiring inside the yoke, which could interfere with surgical procedures.
Check if your Dual Flat Panel Monitor accessory has a serial number listed in the recall: 0416920048, 0417820084, 0417820088, and other specific numbers.
The recall does not specify a remedy, so contact Steris Corporation directly for guidance on next steps.
We’ve drafted a message you can send Steris to request your refund or repair — edit it as you like.
Subject: Recall Z-2178-2025 — Steris Steris Hello, I own a Steris that is covered by recall Z-2178-2025 from Steris. 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.
