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U.S. Department of Health and Human Services

Class 1 Device Recall HAMILTON Intensive Care Ventilator

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  Class 1 Device Recall HAMILTON Intensive Care Ventilator see related information
Date Initiated by Firm June 27, 2022
Create Date August 19, 2022
Recall Status1 Open3, Classified
Recall Number Z-1525-2022
Recall Event ID 90576
510(K)Number K201658  
Product Classification Ventilator, continuous, facility use - Product Code CBK
Product HAMILTON-C6 Intensive Care Ventilator, REF: 160021
Code Information UDI-DI: 07630002808590, Serial Numbers: 5663, 6995, 6907, 6952, 7177, 7772, 6932, 6157, 8658, 7307, 5939, 6858, 6231, 8620, 6349, 8356, 6480, 8322, 8306, 9100, 9101, 9099, 9098, 6219, 7894, 7861, 8003, 6723, 7802, 4833, 7265, 7980, 7666, 7382, 6774, 7358, 7719, 6896, 6925, 9073, 9062, 9298, 9294, 9301, 9292, 9293, 9290, 9300, 9299, 9291, 9231, 9132, 9108, 8310, 8604, 8255, 8599, 7156, 8313, 8344, 8590, 8087, 8348, 8490, 8151, 7174, 8594, 8477, 8122, 8063, 9353, 9230, 9329, 9243, 9235, 9236, 9337, 9228, 9224, 9229, 9225, 9103, 8413, 6149, 8178, 8401, 7827, 8406, 8409, 7826, 6416, 7831, 6280, 9128, 9260, 9257, 9125, 9120, 9259, 9258, 9354, 8325, 8297, 7777, 6212, 6516, 6871, 8099, 6562, 8258, 5679, 5681, 7808, 7115, 8601, 7349, 7130, 6658, 7581, 7819, 8346, 6537, 8235, 7410, 6868, 8049, 8281, 7966, 7787, 9241, 9242, 9054, 9075, 9131, 9121, 9137, 9134, 9133, 9118, 6350, 7122, 7117, 6790, 7614, 8121, 7884, 8102, 8720, 8715, 8726, 8718, 8719, 9248, 9244, 9127, 9138, 9126, 8256, 8371, 9107, 9109, 9036, 9110, 9069, 9063, 9067, 8097, 9129, 9130, 9459, 8723, 8722, 8713, 8702, 8725, 8714, 8727, 8706, 8517, 8717, 7822, 8148, 7695, 8261, 7165, 6944, 7420, 6937, 7150, 6953, 7201, 6965, 7004, 7196, 8849, 8597, 8850, 9106, 9192, 9239, 9237, 9233, 8311, 7898, 7893, 6641, 6505, 6075, 7986, 8005, 7888, 7887, 9535, 9579, 9508, 9576, 9553, 9577, 9578, 9545, 9582, 9590, 9575, 7845, 7740, 8082, 8070, 6671, 7608, 6566, 8535, 8616, 7821, 6579, 7586, 7994, 7066, 7138, 9102, 9105, 14784, 8603, 8846, 8844, 8847, 8845, 8115, 7113, 7809, 7938, 7993, 7252, 8568, 7754, 7033, 8052, 6829, 8249, 9077, 9080, 9076, 9051, 9064, 9081, 9050, 9071, 9091, 7836, 7656, 9124, 9462, 9297, 9325, 9303, 8866, 9348, 9352, 9324, 9227, 6093, 6159, 6274, 6276, 6309, 6320, 6327, 6464, 6512, 6545, 6674, 6789, 7136, 7173, 7191, 7273, 7279, 7422, 7432, 7569, 7572, 7587, 7644, 7676, 7782, 7783, 7784, 7786, 7788, 7789, 7790, 7792, 7793, 7794, 7795, 7796, 7797, 7798, 7799, 7801, 7806, 7807, 7812, 7813, 7837, 7901, 7923, 7969, 8182, 8343, 8394, 8395, 8399, 8420, 8421, 8422, 8423, 8424, 8497, 8519, 8593, 8661, 8668, 8670, 8673, 8675, 8676, 8678, 8707, 8709, 8712, 9028, 9029, 9032, 9033, 9042, 9043, 9044, 9046
Recalling Firm/
Manufacturer		 Hamilton Medical AG
Via Crusch 8
Bonaduz Switzerland
For Additional Information Contact
41816606010
Manufacturer Reason
for Recall		 Ventilator status indicator board can become loose, which could lead to water ingress (disinfectants) that may lead to technical fault alarms. Multiple technical faults in a short time may force ventilators into Safety Ventilation (blower runs constantly) or Ambient Sate (inspiratory channel/expiratory valves opened; patient breaths room air unassisted) with Panel connection lost message displayed
FDA Determined
Cause 2		 Device Design
Action On 6/27/22 Field Safety Notices were emailed to health care facilities, distributors, and service engineers who were informed to take the following actions: 1) In case of a loose status indicator board observed by the user, the front housing containing the status indicator board shall be replaced. This replacement prevents the water ingress that may lead to ambient state. 2) Check your affected ventilator and inform the distributor immediately if you detect the loosening of the status indicator board. 3) Your local distributor or service engineer will contact you shortly. 4) Loose status indicator board may not lead immediately to an ambient state, however it shall be replaced immediately to avoid any risk to the patient. 5) According to the Operator s manual, make sure to always have an alternative means of ventilation available when using ventilation devices. 6) Complete and return the confirmation sheet. Customers with questions can contact the firm: +41 58 610 10 20, techsupport@hamilton-medical.com
Quantity in Commerce 358
Distribution US nationwide distribution including Puerto Rico.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database 510(K)s with Product Code = CBK and Original Applicant = Hamilton Medical AG
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