DR 800. Digital Radiography X-ray System.
Reported: September 4, 2024 Initiated: July 29, 2024 #Z-2738-2024
Product Description
DR 800. Digital Radiography X-ray System.
Reason for Recall
Potential for the front lever chain of the DR 800 table to fail.
Details
- Recalling Firm
- Agfa N.V.
- Units Affected
- 141 units
- Distribution
- Worldwide - US Nationwide distribution in the states of CA, FL, IL, IN, KS, LA, MA, MO, NJ, NC, OH, OK, SC, VA, WV, WI; and the countries of AU, BE, BW, CA, CO, CZ, DE, ES, FR, GB, GR, IL, IN, IT, KZ, MX, PL, RS, UZ, ZA.
- Location
- Mortsel
Frequently Asked Questions
What product was recalled? ▼
DR 800. Digital Radiography X-ray System.. Recalled by Agfa N.V.. Units affected: 141 units.
Why was this product recalled? ▼
Potential for the front lever chain of the DR 800 table to fail.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 4, 2024. Severity: Moderate. Recall number: Z-2738-2024.
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