AQURE System Software Version 2.2.0 recall
AQURE System Software Version 2.2.0 Model #: 933-599 UDI: (01)05700699335999(10)2.2.0 Catalog number: 933-599 The AQURE system manages Radiometer…
Why was AQURE System Software Version 2.2.0 recalled?
Design error when displaying additional information in the patient view window; error may result in misreading a parameter and its value.
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?
UDI: (01)05700699335999(10)2.2.0
- Product
- AQURE System Software Version 2.2.0 Model #: 933-599 UDI: (01)05700699335999(10)2.2.0 Catalog number: 933-599 The AQURE system manages Radiometer…
- Recalling firm
- Radiometer America Inc
- Quantity
- 7 total (2 in US)
- Distribution
- Worldwide Distribution - US including MI and NY and Internationally to England, Switzerland, and United Arab Emirates.
- Recall date
- December 28, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)