IntroMedic Co Miriam Capsule Endoscope System recall — FDA Z-1615-2018
When a user switches on MR1100 Receiver, even though the battery was fully charged, the LED was displayed as orange color due to momentary drop of battery voltage.
Overview of recall records associated with IntroMedic Co., Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 1.
When a user switches on MR1100 Receiver, even though the battery was fully charged, the LED was displayed as orange color due to momentary drop of battery voltage.
This page summarizes recall records in which the official source identifies IntroMedic Co., Ltd. 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.