Recall Z-0309-2027 ยท ODG Endoscopic Ultrasound System, Gastroenterology-Urology
Pentax of America Inc
PENTAX Medical Ultrasound Endoscope. Model Number. EG-3270UK.
| Date | Oct 28, 2026 (initiated Sep 9, 2026) |
| Status | Open, Classified |
| Reason | Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure. |
| Root cause | Unknown/Undetermined by firm |
| Action | An Urgent Field Safety Notice dated 09/02/2026 was mailed to consignees. The notice informs consignees of two updates to the IFU of PENTAX Medical products, specifically the ultrasound endoscope devices and water bottle assembly. Consignees are to inform their staff of this notice and include the warning and updates to their IFUs. Additionally, consignees are instructed to change water for each procedure and fill the bottle approximately 2/3 full, or to the 200 marking on the bottle scale, with sterile water. If the water/balloon feeding function does not work consignees are to fill the water |
| Quantity | 65 units |
| Distribution | Worldwide - US Nationwide and International distribution - Pending. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K182004 | PENTAX Medical Endoscopic Ultrasound System Pentax of America, Inc., Aug 21, 2018 |