{ "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": "2026-09-05", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "220982", "product_res_number": "Z-2950-2026", "event_date_initiated": "2026-05-13", "event_date_posted": "2026-08-14", "recall_status": "Open, Classified", "res_event_number": "99176", "product_code": "FFX", "k_numbers": [ "K183072" ], "product_description": "EndoFLIP System that includes:\nENDOFLIP 1 SYSTEM EF-100\n05391530810050\n10884521809307\nREFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1\n10884521808096\n05391530810166\nDL ENDOFLIP 1\n10884521786684", "code_info": "ENDOFLIP 1 SYSTEM EF-100\n05391530810050\n10884521809307\nREFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1\n10884521808096\n05391530810166\nDL ENDOFLIP 1\n10884521786684", "firm_fei_number": "3004904811", "recalling_firm": "Covidien, LLC", "address_1": "3062 Bunker Hill Ln", "city": "Santa Clara", "state": "CA", "postal_code": "95054-1105", "additional_info_contact": "Sabrina Zimring\n508-261-8000", "reason_for_recall": "Due to products are incorrectly flagged as expired due to the system's 24-hour usage limit, rendering the product unavailable for clinical procedures.", "root_cause_description": "Under Investigation by firm", "action": "On 05/13/2026, an \"URGENT: MEDICAL DEVICE CORRECTION\" letter was emailed/mailed to inform customer that EF-100 modules are affected by an end-of-life (EOL) software issue that prevents the units from recognizing Endoflip and Esoflip catheters after 01-January-2026, causing them to appear as expired.\n\nOn 07/145/2026, an \"Update to Urgent: Medical Device Correction\" letter was sent via UPS 2-Day delivery updated potential patient harms\n\nCustomers are instructed that:\n\"May use the EF-300 system, if they have one. It is recommended to consult their biomedical staff for assistance in adjusting the internal clock. Instructions for this process are enclosed with this notification. As the product has reached end-of-life and end-of-service, Medtronic Technical Services is unable to assist in resetting the internal clock.\nThe user is advised that effects of the data change workaround are seen in exported files. When a USB drive is inserted into the EF-100 system, the SAVE button is enabled to record raw data. For each procedure, a folder is generated and is automatically deleted when the next procedure begins. The folder name includes the Patient ID, the date (YYMMDD format), and the time (HH:MM). All files generated within this folder include the Patient ID in their filenames. The live data file contains raw data with time stamps. These timestamps will reflect the system date, which, under the Date Change Workaround, will be set to 2020.\n\n\"Post this notice in all care environments where the affected products are used, to maintain awareness to this issue.\n\"Share this notice with all relevant personnel within your organization, and with any organization to which the affected product listed in the Product Information table above has been transferred or distributed.\n\"Complete and return the enclosed Customer Confirmation Form to [insert e-mail], even if you do not have any affected product in your inventory, to acknowledge that you have read and understand this letter.", "product_quantity": "327", "distribution_pattern": "Worldwide - U.S. Nationwide distribution including in the states of AK, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NH, NJ, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, and WV. The countries of Argentina, Australia, Austria, Belgium, Canada, Colombia, Costa Rica, Denmark, France, Germany, Hong Kong, Ireland, Israel, Italy, Netherlands, New Zealand, Northern Ireland, Norway, Portugal, South Korea, Spain, Sweden, Switzerland, United Kingdom.", "openfda": { "k_number": [ "K062222", "K010130", "K012232", "K900058", "K880581", "K190208", "K905154", "K181750", "K920664", "K160725", "K831347", "K832869", "K102214", "K082056", "K990441", "K011472", "K151086", "K231861", "K031169", "K003580", "K031084", "K991288", "K121014", "K973844", "K984444", "K120524", "K921682", "K181760", "K252605", "K932306", "K092850", "K874690", "K120997", "K122294", "K000386", "K013154", "K071094", "K991389", "K011471", "K004040", "K102801", "K223705", "K760761", "K942247", "K130906", "K183072", "K191087", "K830421", "K060166", "K091070", "K240007", "K921062", "K222000", "K980980", "K981733", "K780812", "K160170", "K881609", "K980946", "K170833", "K201106", "K823701", "K160287", "K812103", "K992713", "K052338", "K002427", "K963064", "K972439" ], "device_name": "System, Gastrointestinal Motility (Electrical)", "medical_specialty_description": "Gastroenterology, Urology", "regulation_number": "876.1725", "device_class": "2", "registration_number": [ "8020893", "1836324", "9611896", "2023374", "3016854619", "3012302888", "9611668", "3008717264", "3010381606", "9681384", "3010082909", "3018094310", "3017448360", "3009106214", "3012480535", "1126271", "3016544248", "3008414621", "3004904811", "3013973539", "3035451914", "3009445917", "3015198783", "3002821211", "3008361498", "3007662958", "3011790297", "3002806603", "9710107", "1123137", "1119033" ], "fei_number": [ "3003348376", "1000263641", "2023374", "3016854619", "3012302888", "3009293069", "3008717264", "3010381606", "3010082909", "3018094310", "3017448360", "3009106214", "3012480535", "3002807626", "3016544248", "3008414621", "3004904811", "1000123180", "3013973539", "3035451914", "3015198783", "3002821211", "3008361498", "3007662958", "3002807135", "3002807850", "3011790297", "3002806603", "3002998595", "1119033", "3002957361" ] } } ] }