Proteus 235 recall
Proteus 235, graphite block 8
Why was Proteus 235 recalled?
IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader
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?
PAT.115, SAT.116
- Product
- Proteus 235, graphite block 8
- Recalling firm
- Ion Beam Applications S.A.
- Quantity
- 3
- Distribution
- WA
- Recall date
- March 14, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)