Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Prosound F75 or F75 The Hitachi Aloka Medical Recalled by Hitachi Aloka Medical, Ltd. Due to Loosened monitor arm.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hitachi Aloka Medical, Ltd. directly.
Affected Products
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
Why Was This Recalled?
Loosened monitor arm.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hitachi Aloka Medical, Ltd.
Hitachi Aloka Medical, Ltd. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report