Recall Z-1188-2016— Richard Wolf Medical Instruments Corp.
Class II · Terminated
Class II FDA medical device recall by Richard Wolf Medical Instruments Corp., initiated 2016-02-29, terminated 2019-07-03. FDA's recall record names no specific 510(k) clearance for this event. Product: The Vesa 75/100 adaptation with rotation is an accessory to a surgical camera intended to be used to record operative procedures.. Reason: Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of their monitor mounts and support arms may be missing riveting..
- Recalling firm
- Richard Wolf Medical Instruments Corp.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-02-29
- Terminated
- 2019-07-03
- Firm location
- Vernon Hills, IL, United States
Product description
The Vesa 75/100 adaptation with rotation is an accessory to a surgical camera intended to be used to record operative procedures.
Reason for recall
Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of their monitor mounts and support arms may be missing riveting.
Data sourced from openFDA. This site is unofficial and independent of the FDA.