Capintec Inc

Complete recall history across all FDA and CPSC categories — 4 total recalls

Capintec Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (4)

FDA medical device enforcement actions by Capintec Inc

Date Product Reason Class
Mar 3, 2020 Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 -... It is possible that the collimators have screw hole locations that were insuf... Class II
Nov 5, 2018 Captus 3000 Thyroid Uptake System, Model # 5430-0076 and 5430-0077 There is a potential for the spring arm failure as a result of a broken tensi... Class II
Nov 5, 2018 Captus 700 Thyroid Uptake System, Model # 5430-3137 and 5430-3138 There is a potential for the spring arm failure as a result of a broken tensi... Class II
Jul 24, 2012 Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended ... Customers who received a Capintec Captus 3000 Thyroid Uptake System with Soft... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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