Integra recalls C7000 Clarity Ultrasonic Tissue Ablation System's 36 kHz Sterilization Tray due to insufficient drying time in 30-minute cycles, risking incomplete sterilization.
The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not meet the Dry Time Criteria for a 30-minute drying cycle. The current CUSA Clarity Operators manual states 30 minutes for the minimum Dry Time for the 36 kHz Sterilization Tray and 36 kHz Components but 40 minutes is required for complete drying.
Integra is recalling the C7000 Clarity Ultrasonic Tissue Ablation System's 36 kHz Sterilization Tray because it doesn't dry properly in 30-minute cycles as required. This could lead to incomplete sterilization, potentially causing infections during medical procedures.
The sterilization tray requires 40 minutes for complete drying but the system's manual states 30 minutes. This mismatch means the tray may not dry fully, leading to incomplete sterilization and potential infection risks during medical procedures.
Healthcare professionals using the C7000 Clarity system with the specific 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) are most at risk. Patients undergoing procedures with this equipment could face infection risks if sterilization is incomplete.
Check for the 36 kHz Sterilization Tray model C7136 Rev C or 72904491 Rev A in the C7000 Clarity Ultrasonic Tissue Ablation System. The Japanese OPS Manual with part number 60905776 is also associated with this recall.
Identify if your tray is model C7136 Rev C or 72904491 Rev A from the C7000 Clarity system.
The tray does not meet the required 40-minute drying time for complete sterilization, as the system's manual states only 30 minutes.
The recall record does not specify a remedy or action steps for affected users.
The hazard involves potential incomplete sterilization, which could lead to infection risks during medical procedures.
We’ve drafted a message you can send Integra LifeSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-0629-2020 — Integra LifeSciences Integra LifeSciences Hello, I own a Integra LifeSciences that is covered by recall Z-0629-2020 from Integra LifeSciences. 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.
