Z-1559-2022 Class II Terminated
FDA device recall Z-1559-2022 was initiated by Aizu Olympus Co., Ltd. on Jul 20, 2022 and is designated Class II. Reason for recall: The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner. The recall status is terminated (terminated Jan 22, 2025).
Recall Details
- Product Type
- Devices
- Report Date
- Aug 31, 2022
- Initiation Date
- Jul 20, 2022
- Termination Date
- Jan 22, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
Product Description
EVIS EXERA III Bronchovideoscope
Reason for Recall
The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.
Distribution Pattern
US Nationwide distribution in the states of FL, IL, NC, PA & TX.
Code Information
UDI-DI: 04953170342134; Serial No. 2911858; Model No. BF-XP190.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1559-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026