[Recalled] Ultrasound Gastroscope Product Usage: Intended to provide optical visualization of, ultrasonic Visualization of, and therapeutic access to the Upper Gastrointestinal Tract including but not restricted to, the organs; tissues;
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Ultrasound Gastroscope Product Usage: Intended to provide optical visualization of, ultrasonic Visualization of, and therapeutic access to the Upper Gastrointestinal Tract including but not restricted to, the organs; tissues; and subsystems: Esophagus, Stomach, Duodenum, Small Bowel and underlyi |
|---|---|
| Brand / manufacturer | Pentax Medical Company |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2279-2016 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 06 April 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable Pentax Medical water bottle assembly (OS-H4) which has not been cleared for use with this devices in the United States.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Pentax Medical Company
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.