Drug recall

Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664

FDA recall event 83171 · Class II · Olympus Corporation of the Americas

Key facts

Event ID 83171
Recall numbers Z-1983-2019
Recalling firm Olympus Corporation of the Americas
Product type Devices
Products Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
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.
Initiation date Jun 10, 2019
Report date Jul 24, 2019
Termination date Jul 10, 2020
City Center Valley
State PA
Country United States
FEI number 2429304

At a glance

  • 1–9 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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