Shimadzu recall
Shimadzu, Trinias, Digital Angiography System
Why was Shimadzu recalled?
Due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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 Number: 41EFFF7D3001/UDI: (01)04540217058020
- Product
- Shimadzu, Trinias, Digital Angiography System
- Recalling firm
- SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
- Quantity
- 1
- Distribution
- US Nationwide distribution in the states of OH.
- Recall date
- March 20, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)