{ "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": "190025", "product_res_number": "Z-0307-2022", "event_date_initiated": "2021-10-22", "event_date_created": "2021-11-25", "recall_status": "Open, Classified", "res_event_number": "88923", "product_code": "KDQ", "k_numbers": [ "K043582" ], "product_description": "The Ocean Water Seal Chest Drain is a plastic, three bottle vacuum collection device. It consists of a collection chamber that holds shed mediastinal blood, a water seal chamber using a water seal that prevents air from entering into the pleural space and a suction control chamber, which incorporates a mechanical regulator to control suction pressures imposed upon the patient's pleural cavity.", "code_info": "Product Code/REF Number 2002-400; Lot codes: 441533, 443300, 443608, 443629, 444473, 445527, 448966, 449683, 450899, 450900, 451270, 451988, 452177, 452814, 454577, 455871, 458264, 458604, 459198, 459642, 462192, 462194, 464075, 464076, 465037, 466247, 469921, 470627, 471651,471703, 472562, 472785 and 473725.  UDI Code: 00650862100211", "firm_fei_number": "3011175548", "recalling_firm": "Atrium Medical Corporation", "address_1": "40 Continental Blvd", "city": "Merrimack", "state": "NH", "postal_code": "03054-4332", "additional_info_contact": "SAME\n603-880-1433", "reason_for_recall": "Inadequate/inappropriate Set-Up Instructions, which may result in delay in treatment and an unreasonable risk of harm to the patient", "root_cause_description": "Labeling design", "action": "Atrium/Getinge issued Urgent Medical Device Correction letter issued October 22, 2021 via FedEx 2 day delivery. Letter states reason for recall, health risk and action to take:\nOur records indicate that you have received the Ocean Water Seal Chest Drain, Product Code/REF number 2002-400, having the lot numbers that are affected by this correction. \n\nPlease ensure that all Ocean Water Seal Chest Drain, Product Code/REF number 2002-400, users at your facility are aware of this notice and post a copy of the Product Correction Notification on Page 4 in all inventory locations within your facility where the Atrium Ocean Chest Drains are stored.\n\nPlease examine your inventory immediately to determine if you have any of the Ocean Water Seal Chest Drain, Product Code/REF number 2002-400, with the lot numbers listed in this notice.\n\nPLEASE FORWARD THIS INFORMATION TO ALL CURRENT AND POTENTIAL OCEAN CHEST DRAIN USERS WITHIN YOUR HOSPITAL / FACILITY.\n\nIF YOU ARE A DISTRIBUTOR WHO HAS SHIPPED ANY AFFECTED PRODUCTS TO CUSTOMERS, PLEASE FORWARD THIS DOCUMENT TO THEIR ATTENTION FOR APPROPRIATE ACTION.\n\nPlease complete and sign the attached MEDICAL DEVICE CORRECTION - RESPONSE FORM (page 5) to acknowledge that you have received this notification. Return the completed form to Atrium/Getinge by e-mailing a scanned copy to oceandrain.atrium@getinge.com or by faxing the form to (877) 448-0547.\nf you have any questions, please contact your Atrium/Getinge representative or call Atrium/Getinge Customer Support at (603) 880-1433 (press option 1), Monday through Friday, between the hours of 8:00 a.m. and 6:00 p.m. (Eastern Time Zone).", "product_quantity": "87,972 drains (14,662 cases; 6 units/case)", "distribution_pattern": "US Nationwide Distribution\nForeign:\nBahrain\nBelgium\nBrunei Darussalam\nCanada\nColombia\nEcuador\nFinland\nItaly\nKuwait\nLibya\nMauritius\nMexico\nNetherlands\nPoland\nPortugal\nRussian Federation\nSaudi Arabia\nSpain\nUnited Arab Emirates\nUnited Kingdom of Great Britain and Northern Ireland", "openfda": { "k_number": [ "K062302", "K810892", "K800861", "K896127", "K962168", "K811955", "K896697", "K811192", "K802174", "K812746", "K984496", "K897125", "K801221", "K844853", "K855074", "K881149", "K882468", 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"General Hospital", "regulation_number": "880.6740", "device_class": "2" } } ] }