{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-08-20", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "177758", "product_res_number": "Z-0637-2020", "event_date_initiated": "2019-10-21", "event_date_created": "2019-12-08", "recall_status": "Terminated", "event_date_terminated": "2020-05-07", "res_event_number": "84216", "product_code": "LFL", "k_numbers": [ "K182809" ], "product_description": "C7000 - CUSA Clarity Ultrasonic Tissue Ablation System", "code_info": "Brazilian OPS Manual  P/N 60905780", "firm_fei_number": "3003418325", "recalling_firm": "Integra LifeSciences Corp.", "address_1": "311 Enterprise Dr", "city": "Plainsboro", "state": "NJ", "postal_code": "08536-3344", "additional_info_contact": "Dr. Patricia Kihn\n717-309-3966", "reason_for_recall": "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.", "root_cause_description": "Device Design", "action": "All impacted consignees (Hospitals, Distributors and Sales reps) were notified by letter delivered by courier service (2nd day), facsimile or email between October 21st and 23rd, 2019.\nURGENT: VOLUNTARY MEDICAL DEVICE CORRECTION\nCUSA Clarity Operators Manual\n\nDear Valued Customer/Distributor:\nThe purpose of this letter is to advise you that Integra LifeSciences is voluntarily conducting this field corrective action for the Operators Manuals associated with C7000 CUSA Clarity Console. It was discovered through internal review that we need to revise the Operators Manual to reflect the most accurate sterilization parameters and hence the dry time parameters have been changed from 30 minutes to 40 minutes for the CUSA Clarity 36kHz handpiece and components consistent with the CUSA Clarity 23kHz handpiece and components.\n\nThere is an improbable likelihood that serious injuries could occur due to the corrections identified within this field action. The internal review confirms that there have been no adverse events or complaints that Integra LifeSciences is aware of associated with the dry cycle time noted in the current Operators Manuals, nor have there been any reports of serious injuries or deaths related to this issue.\n\nWhile it is highly unlikely that a shortened dry time will result in a non-sterile product given that the drying occurs after the steam application, it may result in visible moisture (most likely on the outer wrap). Sterilization Dry Time moisture may be detected by inspection of components and the outer wrap for visible moisture or water. Where visible moisture is noted the product should be re-wrapped and re-sterilized.\n\nWe request you take the following actions:\n1. Customers\n a. Please review and understand the information provided in Appendix 1.\n b. Review The Sterilization Parameters in Section 11 of your Operators Manual.\n c. Replace the information in Section 11 of your Operators Manual with the information", "product_quantity": "820", "distribution_pattern": "US: AL AR AZ CA CO CT FL GA IA ID IL IN KS KY LA MA MD MI MN MO MS NC NE NJ NY OH OK OR PA SC TN UT VA WA WI WV\n\nInternational: SG MX CA JP AU CO TH HK", "openfda": { "k_number": [ "K191555", "K993868", "K221102", "K901974", "K042277", "K904010", "K894600", "K100597", "K212049", "K153371", "K153299", "K971861", "K991791", "K000095", "K942095", "K211273", "K113570", "K141371", "K230427", "K050776", "K880815", "K933559", "K202299", "K901737", "K133314", "K151340", "K971609", "K893926", "K210567", "K982841", "K990430", "K934628", "K221835", "K132612", "K212301", "K060245", "K801623", "K880814", "K972114", "K081459", "K864983", "K240493", "K221790", "K102258", "K921251", "K960040", "K821820", "K051947", "K970471", "K964742", "K883091", "K020220", "K983199", "K101561", "K042777", "K161882", "K221763", "K950945", "K010309", "K160752", "K012176", 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"regulation_number": "", "device_class": "U" } } ] }