Richard Wolf Medical Instruments Corp. recalls The Vesa 75/100 adaptation with rotation is an accessory to a surgical camera intended to be used to record operative p…
- Recall date
- February 29, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1188-2016
- FDA classification
- Class II
- Brand / firm
- Richard Wolf Medical Instruments Corp.
- Sold / distributed
- Nationwide Distribution including Virginia, Pennsylvania, Florida, California, Texas, North Carolina and Illinois.
Why it was recalled
Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of their monitor mounts and support arms may be missing riveting.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
The Vesa 75/100 adaptation with rotation is an accessory to a surgical camera intended to be used to record operative procedures.
Get recall alerts
Free email alert whenever Richard Wolf Medical Instruments Corp. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Richard Wolf Medical Instruments Corp.