AVID Medical, Inc. recalls Halyard KNEE ARTHROSCOPY PACK - Medical convenience kits Model Number: MAMC204-16
- Recall date
- September 20, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0410-2025
- FDA classification
- Class II
- Brand / firm
- AVID Medical, Inc.
- Sold / distributed
- US Nationwide distribution.
Why it was recalled
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Halyard KNEE ARTHROSCOPY PACK - Medical convenience kits Model Number: MAMC204-16
Get recall alerts
Free email alert whenever AVID Medical, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: AVID Medical, Inc.