AMX Navigate Mobile X-Ray System recall
AMX Navigate Mobile X-Ray System
Why was AMX Navigate Mobile X-Ray System recalled?
An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system.
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?
AMXNV2000001WK, AMXNV2000002WK, DF2401600003WK
- Product
- AMX Navigate Mobile X-Ray System
- Recalling firm
- GE Healthcare, LLC
- Quantity
- 3 units
- Distribution
- Domestic Distribution Only
- Recall date
- October 6, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)