ArthroCare Medical EVAC 70 XTRA with Integrated Cable REF EICA5872-01 Product Usage: PLASMA recall — FDA Z-1832-2015
Potential component failure causing device inoperability
Overview of recall records associated with ArthroCare Medical Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 4.
Potential component failure causing device inoperability
Potential component failure resulting in inoperability
The recalling firm was notified by the contract manufacturer that they had reversed the L2, L3, L4, or L5 components on the P/N09010 RoHS boards of the Coblator II Controller (Model…
Potential breach of sterile barrier due to defective product tray.
This page summarizes recall records in which the official source identifies ArthroCare Medical Corporation as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.