There is a complaint regarding internal check cable recall
There is a complaint regarding internal check cable guide mechanism failure for the Nucletron Flexitron brachytherapy afterloader system. Due to an…
Why was There is a complaint regarding internal check cable recalled?
A component failure may lead to treatment interruption or incorrect source positioning.
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?
REF 136149A02; UDI: (01)08717213051126 (11)171127 (21)FT00340 (240)136149
- Product
- There is a complaint regarding internal check cable guide mechanism failure for the Nucletron Flexitron brachytherapy afterloader system. Due to an…
- Recalling firm
- Nucletron BV
- Quantity
- 383
- Distribution
- Distribution in United States and worldwide
- Recall date
- January 8, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)