PlainRecalls
FDA Devices Moderate Class II Ongoing

Captus 4000e Thyroid Uptake System with Well. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.

Reported: June 5, 2024 Initiated: April 22, 2024 #Z-1893-2024

Product Description

Captus 4000e Thyroid Uptake System with Well. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.

Reason for Recall

Complaints of unexpected detachment of the collimator have been reported.

Details

Units Affected
1,275 units
Distribution
Worldwide - US Nationwide distribution and the countries of ALGERIA, AUSTRALIA, AUSTRIA, BANGLADESH, CANADA, CHILE, CHINA, COSTA RICA, CROATIA, FRANCE, GERMANY, GUAM, HONDURAS, HUNGARY, INDIA, ISRAEL, ISREAL, ITALY, JAPAN, KOREA, LATVIA, MALAYSIA, NETHERLANDS, NEW ZEALAND, PAKISTAN, PHILIPPINES, PHILIPPINES , PHILLIPINES, PUERTO RICO, QATAR, SAUDI ARABIA, SERBIA, SOUTH AFRICA, SOUTH KOREA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, TAIWAN , THAILAND, TURKEY, UNITED KINGDOM, VIETNAM.
Location
Florham Park, NJ

Frequently Asked Questions

What product was recalled?
Captus 4000e Thyroid Uptake System with Well. Intended to be used to perform Thyroid Uptakes, Staff Bioassay, and wipe tests.. Recalled by Mirion Technologies (Capintec), Inc.. Units affected: 1,275 units.
Why was this product recalled?
Complaints of unexpected detachment of the collimator have been reported.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 5, 2024. Severity: Moderate. Recall number: Z-1893-2024.