Aeos¿ Robotic Digital Microscope with software versions recall
Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
Why was Aeos¿ Robotic Digital Microscope with software versions recalled?
Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:
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?
GUIDID: 04046955206742 Serial Numbers: 1004; 1026; 1032; 1035; 1036
- Product
- Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
- Recalling firm
- Aesculap Implant Systems LLC
- Quantity
- 5 units
- Distribution
- US Distribution to states of: AR, IN, NE and NC
- Recall date
- August 17, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)