Sensis Vibe Hemo recall
Sensis Vibe Hemo
Why was Sensis Vibe Hemo recalled?
The possibility of the Sensis documentation functionality application to crash.
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?
Model No. 11007641; UDI-DI 04056869010199; Serial No. 18009, 106245, 18016, 18014, 18011, 18010, 19001, 106244, 18015.
- Product
- Sensis Vibe Hemo
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 331 units
- Distribution
- Domestic: CA, CT, & FL.
- Recall date
- January 17, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)