Z-2621-2017 Class II Terminated
FDA device recall Z-2621-2017 was initiated by Omega Medical Imaging, Inc. on March 23, 2017 and is designated Class II. Reason for recall: Elevating Monitor Suspension column dropping and will not rise back up. The recall status is terminated (terminated December 11, 2019). Affected quantity: 6 units.
Recall Details
- Product Type
- Devices
- Report Date
- June 28, 2017
- Initiation Date
- March 23, 2017
- Termination Date
- December 11, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 6 units
Product Description
Omega Medical Imaging - 2 over 2 Elevating Monitor Suspension pillar/column accessory Device accessory that elevates monitor for healthcare professionals.
Reason for Recall
Elevating Monitor Suspension column dropping and will not rise back up.
Distribution Pattern
Worldwide Distribution -US Distribution to states of: IN, OH, PA, and MT; and country of: Pakistan.
Code Information
SKF Telescopic Pillar P/N ending in -003