FDA Device recall Z-1878-2018
Trident Endoscopic Ultrasonic Aspiration Needle (FNA)
- FDA Device
- Class II
- terminated
- Published 2018-05-23
On 2018-05-23 the FDA classified a Class II recall of Trident Endoscopic Ultrasonic Aspiration Needle (FNA) by Micro Tech Nanjing, citing the combination of the firmness of the mass, the potential endoscope and elevator position combined with the force required to penetrate the mass may contribute to the breakage of….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1878-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-12 |
| Published | 2018-05-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Micro Tech Nanjing |
| Distribution | MI |
Product
Trident Endoscopic Ultrasonic Aspiration Needle (FNA)
Reason
The combination of the firmness of the mass, the potential endoscope and elevator position combined with the force required to penetrate the mass may contribute to the breakage of the needle in the human body, which could cause injury.
Identifiers
| code_info | Identifier EUS-22-0-N UPN ES34601 M171226172 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1878-2018%22
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