Medical Vision Ab Double Pump RF Patient Cassette recall — FDA Z-2705-2016
Sterility of device may be compromised due to sterile package breakage.
Overview of recall records associated with Medical Vision Ab, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Sterility of device may be compromised due to sterile package breakage.
This page summarizes recall records in which the official source identifies Medical Vision Ab 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.