{ "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": "50557", "product_res_number": "Z-0630-2007", "event_date_initiated": "2006-09-27", "event_date_posted": "2007-03-15", "recall_status": "Terminated", "event_date_terminated": "2007-11-26", "res_event_number": "37442", "product_code": "LJT", "k_numbers": [ "K030083" ], "product_description": "Vaxcel Implantable Vascular Access System - Titanium Mini-Port with PASV Valve and 8F Polyurethane Catheter, REF/Catalog No. 45-215, UPN/Material No. M001452150,", "code_info": "Lots 1137363, 1137364, 1137733, and 1137734", "firm_fei_number": "3017892510", "recalling_firm": "Boston Scientific Corp", "address_1": "10 Glens Falls Tech Park", "city": "Glens Falls", "state": "NY", "postal_code": "12801-3864", "additional_info_contact": "Ms. Cindy Finney\n508-683-4678", "reason_for_recall": "Sterile barrier may have been compromised. Firm received one complaint which demonstrated that the inner and outer seals of the port tray packaging had been compromised.", "root_cause_description": "Other", "action": "On 9/27/06, Boston Scientific Corp. sent Urgent Medical Device Recall - Immediate Action Required letters (dated 9/27/06) via Federal Express to the 84 end users (medical facilities). The letters informed the users of the recall of the products due to a compromised sterile barrier. The letters instructed the users to immediately remove the affected lots from inventory, segregate them, contact Boston Scientific at 1-800-862-1284 to obtain a Return Authorization (RGA) number, return the product in an appropriate shipping carton, place the label on the outside of the shipping box, write the RGA # on the outside of the shipping carton, and return the recalled product to Boston Scientific Corp. Distribution Center, Attn: QA Returns, 500 Commander Shea Blvd., Quincy, MA 02171. Accompanying each letter was a Reply Verification Tracking Form to be completed by the user, and mailed or faxed back to Boston Scientific.", "product_quantity": "Domestic - 194", "distribution_pattern": "Nationwide", "openfda": { "k_number": [ "K872329", "K964559", "K983480", "K934167", "K993024", "K904077", "K924748", "K861498", "K951076", "K962230", "K840788", "K874184", "K130576", "K882190", "K926139", "K034065", "K950131", "K903220", "K862018", "K830000", "K934796", "K946189", "K950212", "K871209", "K873213", "K870817", "K921475", "K912424", "K101017", "K951872", "K911355", "K082126", "K000125", "K932095", "K974829", "K110407", "K832788", "K992880", "K850888", "K934802", "K932447", "K905844", "K072657", "K964066", "K905850", "K924250", "K242328", "K010189", "K841149", "K913350", "K190559", "K921902", "K964538", "K021580", "K022983", "K153228", "K871192", "K932840", "K260916", "K882230", "K060036", "K851293", "K904417", "K251253", "K880571", "K955819", "K921201", "K905851", 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"3002468371" ], "device_name": "Port & Catheter, Implanted, Subcutaneous, Intravascular", "medical_specialty_description": "General Hospital", "regulation_number": "880.5965", "device_class": "2" } } ] }