Home › Device types › IZD
Probe, Uptake, Nuclear
FDA product code IZD · Class 1 · Radiology
120
Registered devices
55
Adverse events
9
Recalls
30
510(k) clearances
Devices with this code
ATOMLAB — BIODEX MEDICAL SYSTEMS, INC.neoprobe — DEVICOR MEDICAL PRODUCTS, INC.GammaPro Angled Standard Probe — KubtecWPROBE — GENERAL EQUIPMENT FOR MEDICAL IMAGING SAGammaPro Laparoscopic Probe with Tablet and Carry Case — KubtecGammaPro Standard Probe with Tablet Carry Case — KubtecEUROPROBE — EURORADTruNode — Hologic, Inc.Navigator 3 WirelessPprobe, 13mm Straight — crystal-photonics GmbHNavigator 3 Wireless Probe Battery Pack — crystal-photonics GmbHEUROPROBE — EURORADLara Sensor, Type 6 — LUCERNO DYNAMICS, LLCEUROPROBE — EURORADEUROPROBE — EURORADneoprobe — DEVICOR MEDICAL PRODUCTS, INC.GammaPro Laparoscopic Probe — KubtecLara Docking Station — LUCERNO DYNAMICS, LLCLara Sensor, Type 3 — LUCERNO DYNAMICS, LLCLara Sensor, Type 2 — LUCERNO DYNAMICS, LLCneoprobe — DEVICOR MEDICAL PRODUCTS, INC.EUROPROBE — EURORADneoprobe — DEVICOR MEDICAL PRODUCTS, INC.EUROPROBE — EURORADneoprobe — DEVICOR MEDICAL PRODUCTS, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-22 | Mirion Technologies (Capintec), Inc. | Complaints of unexpected detachment of the collimator have been reported. |
| 2024-04-22 | Mirion Technologies (Capintec), Inc. | Complaints of unexpected detachment of the collimator have been reported. |
| 2024-04-22 | Mirion Technologies (Capintec), Inc. | Complaints of unexpected detachment of the collimator have been reported. |
| 2023-11-27 | Mirion Technologies (Capintec), Inc. | Spring arm failure with Captus 4000e Thyroid Uptake Systems, can cause the collimator to fall downward to its lowest point of travel, causing potential injury w |
| 2020-09-07 | Devicor Medical Products Inc | It was discovered during a documentation review that China has the software version as v5.01 approved for use in China. The current software version on devices |
| 2020-03-03 | Capintec Inc | 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 com |
| 2018-11-05 | Capintec Inc | There is a potential for the spring arm failure as a result of a broken tension rod (a component inside the arm). A break in the tension rod can casue the coll |
| 2018-11-05 | Capintec Inc | There is a potential for the spring arm failure as a result of a broken tension rod (a component inside the arm). A break in the tension rod can casue the coll |
| 2012-07-24 | Capintec Inc | Customers who received a Capintec Captus 3000 Thyroid Uptake System with Software Revisions 1.22, 1.23, 1.24, 1.25, and 1.26 may encounter an error while using |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.