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 diagnoses.
Reported: August 20, 2014 Initiated: May 13, 2014 #Z-2176-2014
Product Description
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 diagnoses.
Reason for Recall
Unit was mislabeled with a factory label showing 32 KW output power.
Details
- Recalling Firm
- AGFA Healthcare Corp.
- Units Affected
- 1
- Distribution
- US in the state of WV
- Location
- Greenville, SC
Frequently Asked Questions
What product was recalled? ▼
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 diagnoses.. Recalled by AGFA Healthcare Corp.. Units affected: 1.
Why was this product recalled? ▼
Unit was mislabeled with a factory label showing 32 KW output power.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 20, 2014. Severity: Low. Recall number: Z-2176-2014.
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