Z-1983-2019 Class II Terminated
FDA device recall Z-1983-2019 was initiated by Olympus Corporation of the Americas on June 10, 2019 and is designated Class II. Reason for recall: WM-NP/DP2 workstations could become unstable and may fall over if the control panel arm is mounted with a video monitor weighing more than 19.8 pounds. The recall status is terminated (terminated July 10, 2020). Affected quantity: N/A.
Recall Details
- Product Type
- Devices
- Report Date
- July 24, 2019
- Initiation Date
- June 10, 2019
- Termination Date
- July 10, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- N/A
Product Description
Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664
Reason for Recall
WM-NP/DP2 workstations could become unstable and may fall over if the control panel arm is mounted with a video monitor weighing more than 19.8 pounds.
Distribution Pattern
Nationwide domestic distribution.
Code Information
All serial numbers