Prosound F75 or F75 The Hitachi Aloka Medical recall
Prosound F75 or F75 The Hitachi Aloka Medical, Ltd. Prosound F75 is intended for use by trained personnel (doctor, sonographer, etc.) for the…
Why was Prosound F75 or F75 The Hitachi Aloka Medical recalled?
Loosened monitor arm.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial Numbers: 202M4896 202M4891 202M4893 202M4897 202M4898 202M4894
- Product
- Prosound F75 or F75 The Hitachi Aloka Medical, Ltd. Prosound F75 is intended for use by trained personnel (doctor, sonographer, etc.) for the…
- Recalling firm
- Hitachi Aloka Medical, Ltd.
- Distribution
- Nationwide Distribution to PA, TX, FL, AZ, IN, OH
- Recall date
- April 5, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)