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FDA (Device enforcement)Recalled 2024-08-02class ii

AURIS HEALTH INC: Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005-01R. Monarch Platform (Bronchoscopy), REF: MON-000006, MON-000006-RFB.

Hazard

Endoscopy/bronchoscopy/urology devices may have a strain relief defect with some cart and tower power cords that may cause an electrical short, which may lead to system shutdown, which can lead to prolonged procedure or case conversion, and if the user (e.g., operating room staff) touches exposed wires or conductive fluids in contact with the exposed wires, there is a chance of electrical shock.

Details from the source

Reason for recall: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with some cart and tower power cords that may cause an electrical short, which may lead to system shutdown, which can lead to prolonged procedure or case conversion, and if the user (e.g., operating room staff) touches exposed wires or conductive fluids in contact with the exposed wires, there is a chance of electrical shock. Distribution: Worldwide - US Nationwide distribution including in the states of MN, FL, NC, AK, NJ, NY, VA, WI, AZ, MS, LA, MI, MA, MT, WV, GA, DE, TX, CA, OH, IN, SC, PA, CT, ND, MO, DC, IL, NE, ID, WA, TN, OR, AL, SD, CO, KY, NM, VT, MD and the countries of Canada. Quantity: 176 Lot/code info: Cart Power Cord 20' 14AWG BLK, PN 304-003613-00. Tower Power Cord 20' 14AWG BLK, PN 304-003607-00. REF/UDI-DI/Serial Numbers: MON-000005-01/+B634MON000005010/110024, 13, 110014, 110016, 110040, 110038, 110027, 110035, 110022, 110034, 1806P2, 120170, 110045, 110039, 110049, 110047, 110052, 110030, 110032, 110021, 110043, 110050, 110029, 110033, 110046, 110048, 110018, 110015, 110051, 1806P1, 110012, 14, 110041, 110036; MON-000005-01R/+B634MON00000501R0/110020, 110017, 110031, 110028, 120042, 110013. MON-000006/+B634MON0000060/120088, 120057, 120046, 120058, 120121, 120152, 120015, 120160, 120068, 120167, 120025, 120030, 120044, 120093, 120040, 120063, 120092, 120173, 120036, 120064, 120122, 120056, 120128, 120017, 120089, 120075, 120031, 120169, 120113, 120168, 120055, 120148, 120014, 120060, 120124, 120164, 120123, 120007, 120006, 120004, 120120, 120126, 120082, 120047, 120051, 120020, 120103, 120153, 120108, 120037, 120074, 120005, 120130, 120095, 120096, 120009, 120111, 120022, 120054, 120163, 120027, 120090, 120141, 120072, 120155, 120101, 120143, 120125, 120052, 120100, 120050, 120098, 120045, 120131, 120013, 120105, 120165, 120136, 120029, 120041, 120139, 120137, 120053, 120028, 120034, 120085, 120019, 120049, 120209, 120144, 120161, 120001, 120145, 120127, 120011, 120070, 120076, 120134, 120117, 120077, 120149, 120102, 120002, 120010, 120003, 120023, 120146, 120043, 120071, 120107, 120065, 120116, 120150, 120066, 120166, 120033, 120079, 120008, 120132, 120086, 120032, 1

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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