Agfa Digital Radiography X-Ray System DX-D 100 Product recall: Labeling Error
Agfa Digital Radiography X-Ray System DX-D 100 Product Usage: Is indicated for use in providing diagnostic quality images to aid the physician with…
Why was Agfa Digital Radiography X-Ray System DX-D 100 Product recalled?
Unit was mislabeled with a factory label showing 32 KW output power.
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?
Serial Number A5410000042
- Product
- Agfa Digital Radiography X-Ray System DX-D 100 Product Usage: Is indicated for use in providing diagnostic quality images to aid the physician with…
- Recalling firm
- AGFA Healthcare Corp.
- Quantity
- 1
- Distribution
- US in the state of WV
- Recall date
- August 20, 2014
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)