The Recall Desk
ModerateFDA (Devices)·Z-1141-2026·Announced 2026-01-28

Fetal and maternal monitors recalled over potential cybersecurity issues

Edan Diagnostics is recalling 3,518 units of its Fetal & Maternal Monitor models F6, F9, F6 Express and F9 Express after an FDA letter raising potential cybersecurity issues with the firm's devices.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: Scored 2 because the record cites potential cybersecurity issues raised in an FDA letter, with no stated defect consequence or reported harm.

Plain-English summary

The EDAN Fetal & Maternal Monitor models F6, F9, F6 Express and F9 Express is being recalled by Edan Diagnostics. The record describes the product as follows: the devices are bedside fetal and maternal monitors, used to monitor the physiological parameters of pregnant women including the fetus.

The reason given in the enforcement record is that the firm received an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm's devices.

The record lists 3,518 units, with model, UDI-DI and serial or lot numbers recorded in the enforcement record. Distribution was worldwide, including nationwide in the United States across a range of states listed in the record. The FDA has classified the action as Class II.

The record names no specific defect, consequence or reported harm. Facilities should follow Edan Diagnostics' instructions.

The recalled product

Product
Brand Name: EDAN Product Name: Fetal & Maternal Monitor Model/Catalog Number: F6, F9, F6 Express, F9 Express Product Description: The devices are bedside fetal and maternal monitors, which are used to monitor the physiological parameters of pregnant women including the fetus f
Manufacturer
Edan Diagnostics
Affected units
3,518

Distribution

Distributed nationwide across the United States.

The notice also names 13 states specifically:

Part of a larger recall action

This product is one of 16 recalled by Edan Diagnostics under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 16 products in this recall →