FDA Device recall Z-1696-2017
Prosound F75 or F75 The Hitachi Aloka Medical, Ltd
- FDA Device
- Class II
- terminated
- Published 2017-04-05
On 2017-04-05 the FDA classified a Class II recall of Prosound F75 or F75 The Hitachi Aloka Medical, Ltd by Hitachi Aloka Medical, citing loosened monitor arm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1696-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-11 |
| Published | 2017-04-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Hitachi Aloka Medical |
| Distribution | US |
Product
Prosound F75 or F75 The Hitachi Aloka Medical, Ltd. Prosound F75 is intended for use by trained personnel (doctor, sonographer, etc.) for the diagnostic ultrasound evaluation of Fetal; Abdominal; Intra-operative; Intra-operative (neurosurgery); Laparoscopic; Pediatric; Small Organ; Neonatal Cephalic; Neonatal Cephalic; Trans-rectal; Trans-vaginal; TEE (non-cardiac); Musculo-skeletal; Cardiac Adult; Cardiac Adult TEE; Cardiac Neonatal; Cardiac Pediatric; Cardiac Pediatric TEE; Peripheral Vascular; and Gynecological applications. The device is not indicated for Ophthalmic applications
Reason
Loosened monitor arm.
Identifiers
| code_info | Serial Numbers: 202M4896 202M4891 202M4893 202M4897 202M4898 202M4894 |
|---|
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-1696-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.