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Insighters

Shenzhen Insighters Medical Technology Co., Ltd. · Model 9Fr · UDI-DI 06970831723383

CBI
1
510(k) clearances
1,573
Adverse events (12 deaths)
10
Recalls
36
Facilities

Recalls

DateFirmReason
2024-09-16Ambu Inc.Ambu has received complaints on Ambu VivaSight 2 DLTs regarding hyper angulation of the distal end. The hyper angulation can lead to an increased risk of complications during intub
2022-06-03Ambu Inc.Firm has received complaints on the device concerning leak/rupture of either the bronchial or tracheal cuff. Leakage during procedure could lead to loss of secure airway and will r
2019-10-30Teleflex MedicalThe tracheal and brochial swivel connectors are incorrectly labeled.
2016-12-16Parker MedicalThe product was not functioning as intended. The ventilation to the patient was not disrupted, but the single lung isolation and ventilation did not function as intended.
2015-06-01Teleflex MedicalThe double swivel connector may crack or separate on the endobronchial tube.
2015-06-01Teleflex MedicalThe double swivel connector may crack or separate on the endobronchial tube.
2015-06-01Teleflex MedicalThe double swivel connector may crack or separate on the endobronchial tube.
2015-06-01Teleflex MedicalThe double swivel connector may crack or separate on the endobronchial tube.
2005-02-23Teleflex MedicalThe distal end of the tube may be printed incorrectly, with catalog numbers V5-16037 and 5-16037 stating 'Bronchial - Right' instead of 'Bronchial - Left', and catalog number 5-161
2005-02-23Teleflex MedicalThe distal end of the tube may be printed incorrectly, with catalog numbers V5-16037 and 5-16037 stating 'Bronchial - Right' instead of 'Bronchial - Left', and catalog number 5-161

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.