Trade name: Stonebreaker-Lithotriptor Pneumatic. Technical name: Lithotripsy / Urology / Gatroenterology System. ANVISA registration number: 10330710088. Class of risk: III. Affected Model: Hardware: SBL-KIT1. Accessories and parts: SBP-010500, SBP-010605, SBP-016500, SBP-016605, SBP-020425, SBA-EC, SBA-EL, SBA-PC, SBA-SC and SBC-10 .. affected. Reference SBL-KIT1: 0900270, 0900468, 5054460, 5054461, 5684194, NS5784309, NS5784311, NS5784311, NS5784312, NS5784313, NS5784315, NS5784315, NS5784316, NS5784317, NS5784318, NS5792890, NS5792891, NS5792892, NS5792893, NS5792894, and 5873311X .. SBA Reference -EC: 6241349 .. SBA-PC Reference: 5257852 and 5943831 .. SBA-SC Reference: 5924492 .. SBC-10 Reference: 09020, 4982708, U2462535, U2466275, U2466279, 5296161, 5282743, 5296161, 591920, 5919200, 5919201 , 6292892, 6292896, 6292892, and 6292896. Referring to SBP-010500: 09054, U2467239 and U2476031 .. Reference SBP-010605: U2473998, 5616732, 5676478, 5716379, 5884345, 5898498 .. Reference SBP-016500: 5000020 and 6028035 .. Reference SBP-016605: 09022, U2427745 and U2458178. Reference SBP-020425: U2067690, 5000021, U2467237, U2467241, 5676479, 5898500, 5925167, 6810029, 7081752 and 7378379. 의 안전성 경고

Brazilian data is current through June 2018. All of the data comes from Anvisa, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Brazil.

Immediately discontinue use and segregate the equipment and its accessories and parts to be returned. Remove all affected products from your stock. Dispose of these products in a safe place for return to Handle. If you wish to notify technical complaints and adverse events use the following channels: -Notivisa: Notices of adverse events (EA) and technical complaints (QT) for products subject to Sanitary Surveillance should be made through the NOTIVISA System, through the access: http: //portal.anvisa.gov.br/notivisa; -Handle: Direct notifications to Handle through the email handle@handle.com.br or by telephone (16) 3456-1400. If you wish to notify technical complaints and adverse events use the following channels: Notivisa: Notices of adverse events (AE) and technical complaints (QT) for products subject to Sanitary Surveillance should be made through the NOTIVISA System. To access the System, you must register and select the Health Professional option, if you are a liberal professional or the Institution / Entity option, if you are a professional of an institution / entity. Technovigilance System: Patient or citizen can notify through the Technovigilance System / SISTEC access through the link Additional information: - Date of identification of the problem by the company: 03/27/2018 - Date of notification notice to Anvisa: 04/13/2018 The company that owns the affected product is responsible for contacting its customers in due time. to ensure the effectiveness of the Field Action in progress. It stands out the joint responsibility of the distribution chain and use of health products in maintaining its quality, safety and efficacy, as well as the effectiveness of the Field Action, expressed by RDC 23/2012: "(...) Art 2 ° A holder of registration of health product is the holder of the registration / registration of health product with Anvisa. Single paragraph. The registration holder, as well as other agents involved from the production to the use of the product, or discarding it when applicable, are jointly and severally responsible for maintaining the quality, safety and efficacy of the health products to the final consumer. Art. 12 Distributors of health products shall forward to the registration holder, in a timely manner, the distribution map and other information requested for the notification and execution of field actions. (...) "