{ "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": "114789", "product_res_number": "Z-0621-2013", "event_date_initiated": "2012-11-19", "event_date_posted": "2013-01-03", "recall_status": "Terminated", "event_date_terminated": "2013-07-11", "res_event_number": "63794", "product_code": "BZO", "product_description": "Fisher & Paykel Healthcare reusable breathing circuit.\nNon-heated breathing circuit, 1.8m or 6 feet in length.\n\nOxygen therapy delivery system for adult patient.", "code_info": "Lots 110810 and 111020", "firm_fei_number": "3002806988", "recalling_firm": "Fisher & Paykel Healthcare, Ltd.", "address_1": "15 Marcel Place", "city": "North Shore City", "state": "East Tamaki", "country": "New Zealand", "additional_info_contact": "Derek Arndt\n949-4434095", "reason_for_recall": "FPH has become aware that one batch of tubes supplied to FPH may contain hole damage. These tubes were incorporated by FPH into certain 900MR068 reusable circuits with lot numbers 110810 and 111020. If this hole damage is not detected during the standard leak test before patient use, it could potentially result in a gas leak in the breathing system, which may lead to a loss of pressure for the int", "root_cause_description": "Nonconforming Material/Component", "action": "Fisher & Paykel sent an Urgent Medical Device Recall letter dated November 19, 2012, with a Product Recall Response Form to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to destroy and discard any affected circuits in their possession. Customers were instructed to complete and return the Product Recall Response form to the address indicated on the form, even if they have no affected product. Customers were asked to forward the recall notice to all those who need to be aware within their organization. Customers with questions should call 1-800-792-3912.\nFor questions regarding this recall call 949-443-4095.", "product_quantity": "200 units total, 26 units US", "distribution_pattern": "Worldwide Distribution - USA including IL, IN, AR and GA.", "openfda": { "k_number": [ "K792047", "K922479", "K770593", "K860879", "K823287", "K942569", "K850600", "K850703", "K952012", "K830923", "K830922", "K843036", "K821064", "K772069", "K903055", "K792268", "K792030", "K953784", "K934753", "K834570", "K935582", "K812773", "K863033", "K832681", "K770354", "K833459", "K812774", "K812737", "K841378", "K932712", "K841722", "K874559", "K813155", "K863756", "K791034", "K882341", "K791856", "K823271", "K952022", "K861286", "K896439", "K841637", "K863910", "K880959", "K873927", "K810341", "K903404", "K760993", "K952010", "K911328", "K893760", "K890011", "K830921", "K932560", "K801087", "K823481", "K860659", "K890822", "K932563", "K921510", "K944531", "K791761", "K945740", "K860880", "K850151", "K842778", 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