PlainRecalls
FDA Devices Moderate Class II Terminated

Proteus 235, graphite block 8

Reported: March 14, 2018 Initiated: October 17, 2017 #Z-0930-2018

Product Description

Proteus 235, graphite block 8

Reason for Recall

IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader

Details

Units Affected
3
Distribution
WA
Location
Louvain La Neuve, N/A

Frequently Asked Questions

What product was recalled?
Proteus 235, graphite block 8. Recalled by Ion Beam Applications S.A.. Units affected: 3.
Why was this product recalled?
IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader
Which agency issued this recall?
This recall was issued by the FDA Devices on March 14, 2018. Severity: Moderate. Recall number: Z-0930-2018.