Capintec Inc
Capintec Inc has 3 FDA enforcement events on this register (4 product records) between 2012 and 2020: 3 device; the busiest year was 2012 with 1.
0% of its events are Class I; the most common class is Class II (3). 0 events are listed as ongoing; the recalling firm's address is in NJ and PA.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 3 Mar 2020 | 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. | Device | Class II | 1 | Terminated |
| 5 Nov 2018 | Captus 3000 Thyroid Uptake System, Model # 5430-0076 and 5430-0077 | Device | Class II | 2 | Terminated |
| 24 Jul 2012 | Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended to be used by trained Nuclear Medicine Technologists to perform thyroid uptake procedures, which consist of the measurement of organ uptake and circulating radioactivity. | Device | Class II | 1 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Capintec Inc had?
3 enforcement events (4 product records) on this register, 2012–2020: 3 device.
Are any Capintec Inc recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are Capintec Inc recalls?
3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.