Spes Medica SNS Disposable Urethral Catheter Electrode, 10 Fr, Gold Recording/Stimulating recall — FDA Z-1968-2021
The supplier informed them of possible deviations of the parameters/processes defined for ethylene oxide sterilization.
Overview of recall records associated with Spes Medica, including dates, categories and classifications where available.
Classification mix: Class II: 4.
The supplier informed them of possible deviations of the parameters/processes defined for ethylene oxide sterilization.
The supplier informed them of possible deviations of the parameters/processes defined for ethylene oxide sterilization.
The supplier informed them of possible deviations of the parameters/processes defined for ethylene oxide sterilization.
The supplier informed them of possible deviations of the parameters/processes defined for ethylene oxide sterilization.
This page summarizes recall records in which the official source identifies Spes Medica 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.