FETALGARD Lite Fetal Monitors, Model AP1S (Single Fetus Monitoring) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
FETALGARD Lite Fetal Monitors, Model AP1S (Single Fetus Monitoring)
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
System Serial Numbers: FA002021 FA002022 FA002025 FA002027 FA002033 FA002020 FA002029 FA002005 FA002041 FA002044 FA002046 FA002112 FA002097 FA002117 FA002028 FA002047 FA002048 FA002118 FA002034 FA002093 FA002095 FA002116 FA002008 FA002023 FA002030 FA002031 FA002009 FA002098 FA002040 FA002092 FA002024 FA002114 FA002113 FA002115 FA002026 FA002032 FA001328
A medical device manufacturer is recalling FETALGARD Lite Fetal Monitors, Model AP1S (Single Fetus Monitoring) due to Unit may not power up due to faulty circuit board. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Unit may not power up due to faulty circuit board
Recommended Action
Per FDA guidance
Analogic notified customers by letter dated 9/13/05. Distributors were requested to notify their accounts and return units for replacement of the main circuit board.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CT, PR
Page updated: Jan 10, 2026