FDAClass IIApril 1, 2015

GE Inspection Technologies x|tome|x L240 an Cabinet recall

GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system

Why was GE Inspection Technologies x|tome|x L240 an Cabinet recalled?

It was discovered that the upper left corner-shaped lead shield in the window in one of the doors of the v|tome|x L240 installed had lost adhesion and fall out of position, which could lead to gaps in shielding.

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?

SN - PA1260

Product
GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system
Recalling firm
GE Inspection Technologies, LP
Quantity
2
Distribution
US Distribution to the states of OH and PA.
Recall date
April 1, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
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