GE Cabinet X-ray systems recall
GE Cabinet X-ray systems
Why was GE Cabinet X-ray systems recalled?
GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards.
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?
XXL cabinet x-ray systems, serial numbers A586590 and A586780; xlcube compact cabinet x-ray systems, serial numbers A583730, A586430, and A586460; a VTOMEX C450 cabinet x-ray system, serial number VTXO1JOOO2-2245 14; VTOMEX L300 cabinet x-ray systems, serial numbers VTX01lF007-208813, VTX01F007-196312 and VTXO1FOO07-1946 12; and VTOMEX L450 cabinet x-ray systems, serial numbers VTXO1K0001-184711 and PX_10E000-179013.
- Product
- GE Cabinet X-ray systems
- Recalling firm
- GE Inspection Technologies, LP
- Quantity
- 11
- Distribution
- US Distribution to the states of MI, PA, NH, CA, OR, WA, NC, IN and SC.
- Recall date
- December 24, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)