Merge Hemo with software versions 10.0 LA. Merge Hemo recall: Software Issue
Merge Hemo with software versions 10.0 LA. Merge Hemo (formerly named HeartSuite Hemodynamics) monitors, measures, and records physiologic data from a…
Why was Merge Hemo with software versions 10.0 LA. Merge Hemo recalled?
The firm, Merge Healthcare, sent out Merge HEMO V10.0 & Merge CARDIO V10.1 software to 3 customers before the product was completely validated in house.
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?
Merge Hemo with software versions 10.0 LA
- Product
- Merge Hemo with software versions 10.0 LA. Merge Hemo (formerly named HeartSuite Hemodynamics) monitors, measures, and records physiologic data from a…
- Recalling firm
- Merge Healthcare, Inc.
- Quantity
- 2
- Distribution
- Distributed in the states of IL, NC, and VT.
- Recall date
- January 6, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)