FDA Recall Terminated

Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

Recall: Z-1564-2020 · Initiated March 3, 2020

Recall

Recall Number
Z-1564-2020
Event Number
85237
Firm
Capintec Inc
FEI Number
2518443
Product Code
IZD
Status
Terminated
Root Cause
Device Design
Initiated
March 3, 2020
Posted
March 24, 2020
Terminated
November 12, 2021
Address
7 Vreeland Rd, Florham Park, NJ, 07932-1511

Description

Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

Reason

It is possible that the collimators have screw hole locations that were insufficiently tapped. There is a potential for the collimator assembly to fall and come into contact with a patient or operator.

Action

Important Captus 4000e Safety Notice, Action Required letters dated 3/3/20 were sent to customers. As a precautionary measure, Capintec is requesting customers, whose systems include collimators from the same batch, perform a simple safety inspection. A detailed and easy to follow inspection procedure is included. The inspection can be performed in a few minutes, and any defect would be easily identified. Please confirm completion of inspection process by completing the attached form (page 2) and return to Capintec, Inc. For additional assistance or information, email [email protected] or call 1-800-631-3826 and request technical support. A REVISED March 26, 2020 TO EXTEND SERIAL NUMBER RANGE notification letter was sent to customers: In February 2019, Capintec received a complaint that a collimator fell from a Captus 4000e system. A second complaint of a similar nature was received in September 2019. After evaluation of the failed components, it is possible that the collimators had screw hole locations that were insufficiently tapped. It is believed that the failures occurred after impact to the arm. Both collimators are believed to have originated from the same batch. It is possible other collimators from this batch may have a similar defect. It is also possible that all other collimators from the same batch are without issue and functioning satisfactorily. As a precautionary measure, Capintec is requesting customers, whose systems include collimators from the same batch, perform a simple safety inspection. A detailed and easy to follow inspection procedure is included. The inspection can be performed in a few minutes, and any defect would be easily identified. Please confirm completion of inspection process by completing the attached form (page 2) and return to Capintec, Inc.For additional assistance or information, email [email protected] or call 1-800-631-3826 and request technical support.

Distribution

Worldwide distribution. US Nationwide, Australia, Austria, Bangladesh, Brazil, Canada, Chile, Colombia, Costa Rica, Ecuador, France, Hong Kong, India, Israel, Italy, Korea, Malaysia, Pakistan, Philippines, Poland, Saudi Arabia, Spain, Sweden, Taiwan, Thailand, Turkey, UAE, UK, and Vietnam. (list updated 3/26/2020)

Quantity

48 (481 additional units added 3/26/20)