Reported Sep 23, 2026 · Ongoing · Updated Sep 29, 2026

Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;

Mirion Technologies (Capintec), Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Mirion Technologies (Capintec), Inc. · 7 Vreeland Rd · Florham Park, NJ · 07932-1511

Is this the product you have?

  • Captus 4000e Thyroid Uptake System
  • Models
    • 1. 5430-30151
    • 2. 5430-30152
    • 3. 5430-30154
Lot codes and dates

3 of 3 products

Products covered by this recall
Model / numberBarcodesProduct as published
5430-3015100859942006096UDI-DI: 00859942006096
5430-3015200859942006102UDI-DI: 00859942006102
5430-3015400859942006423UDI-DI: 00859942006423; Devices shipped from April 2019 through February 2024, Serial Numbers 940548 through 941398, that have NOT already replaced the original arm with the redesigned arm.
Amount recalled
783

Where it was sold

  • Nationwide

Why it was recalled

Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from the ground.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 4:57 AM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.