FDA recall Z-0052-2025

AURIS HEALTH INC · Class II · device

Product

Monarch Platform (Urology), REF: MON-000007, MON-000007-RFB

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.

Key facts

Status
Ongoing
Initiation date
2024-08-02
Report date
2024-10-16
Voluntary/Mandated
Voluntary: Firm initiated
Location
Redwood City, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0052-2025