Medical Device Recall: Z-0035-06

FDA Recalls dataset · Firm: N/A · Status: Terminated

Recall Action Class: N/A Date Initiated: 2005-09-13 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0035-06.

Recall Res Number
Z-0035-06
Recalling Firm / Manufacturer
N/A
FEI Number
1220672
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2005-09-13
Date Posted
2005-10-12
Date Terminated
2006-08-07
Product Code
HGM
Event Number
33337
Product Quantity
37 units
Product Description FETALGARD Lite Fetal Monitors, Model AP1S (Single Fetus Monitoring)

Reason for Recall Unit may not power up due to faulty circuit board

Action Details 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.

Distribution Pattern CT, PR Foreign: Algeria, Chile,Ecudor, Mexico, South Africa, Vietnam, Russia, United Arab Emirates, Phillipines, Singapore, Korea, Malyasia

Code Information / Serial Numbers 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

Related Establishments / Registrations

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This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.

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