{"recall":{"id":"fda-device-99729","source":"FDA","sourceName":"U.S. Food and Drug Administration (openFDA device enforcement)","cat":"medicines","kids":false,"kind":"device","title":"Medline Industries, LP recalls 2 products","firm":"Medline Industries, LP","date":"2026-08-10","reported":"2026-09-30","status":"Ongoing","classification":"Class II","products":[{"name":"Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F.","code":"DYNJ48258D UDI-DI 10889942563272 Lots 23CBH459 23GBJ128 24ABM400","quantity":"90 kits (US)","number":"Z-3229-2026","classification":"Class II"},{"name":"Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and SINUS PACK DYNJ48258F.","code":"DYNJ48258F UDI-DI 10198459038334 Lots 24HBR684 25CBS234 25GBH438 25JBC863 26FBU052","quantity":"90 kits (US)","number":"Z-3230-2026","classification":"Class II"}],"reason":"Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards associated include cut injury/abrasion and infection.","hazard":"FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).","affected":"US Nationwide distribution in the states of MN and SD.","nationwide":true,"states":[],"units":"90 kits (US); 90 kits (US)","remedy":"","whatToDo":"Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.","contact":"","url":"https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99729","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","rawHash":"557181dea5d5f0c5","firstSeen":"2026-11-02T13:57:14.206Z","updatedAt":"2026-11-02T13:57:14.206Z","history":[]},"official":{"fetchedAt":"2026-11-02T13:57:14.206Z","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","officialUrl":"https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99729","record":[{"status":"Ongoing","city":"Northfield","state":"IL","country":"United States","classification":"Class II","openfda":{},"product_type":"Devices","event_id":"99729","recalling_firm":"Medline Industries, LP","address_1":"3 Lakes Dr","address_2":"","postal_code":"60093-2753","voluntary_mandated":"Voluntary: Firm initiated","initial_firm_notification":"Letter","distribution_pattern":"US Nationwide distribution in the states of MN and SD.","recall_number":"Z-3229-2026","product_description":"Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F.","product_quantity":"90 kits (US)","reason_for_recall":"Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards associated include cut injury/abrasion and infection.","recall_initiation_date":"20260810","center_classification_date":"20260918","report_date":"20260930","code_info":"DYNJ48258D    UDI-DI 10889942563272    Lots 23CBH459   23GBJ128   24ABM400","more_code_info":""},{"status":"Ongoing","city":"Northfield","state":"IL","country":"United States","classification":"Class II","openfda":{},"product_type":"Devices","event_id":"99729","recalling_firm":"Medline Industries, LP","address_1":"3 Lakes Dr","address_2":"","postal_code":"60093-2753","voluntary_mandated":"Voluntary: Firm initiated","initial_firm_notification":"Letter","distribution_pattern":"US Nationwide distribution in the states of MN and SD.","recall_number":"Z-3230-2026","product_description":"Medline convenience kits containing Healthmark Instrument Channel Brushes.   SINUS PACK DYNJ48258D and SINUS PACK DYNJ48258F.","product_quantity":"90 kits (US)","reason_for_recall":"Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards associated include cut injury/abrasion and infection.","recall_initiation_date":"20260810","center_classification_date":"20260918","report_date":"20260930","code_info":"DYNJ48258F    UDI-DI 10198459038334    Lots 24HBR684   25CBS234   25GBH438   25JBC863   26FBU052","more_code_info":""}]}}