MultiDiagnost-Eleva recall
MultiDiagnost-Eleva
Why was MultiDiagnost-Eleva recalled?
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation
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?
MultiDiagnost-Eleva
- Product
- MultiDiagnost-Eleva
- Recalling firm
- Philips Medical Systems Nederland B.V.
- Quantity
- 5432 systems in total
- Distribution
- US Nationwide Distribution
- Recall date
- September 13, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)