GE Optional Laser Centering Device X-ray generator recall
GE Optional Laser Centering Device X-ray generator.
Why was GE Optional Laser Centering Device X-ray generator recalled?
GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and 21 C.F.R. ¿ 1010.2 for the alignment laser centering device.
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?
Model No. 025.03.00A
- Product
- GE Optional Laser Centering Device X-ray generator.
- Recalling firm
- GE Inspection Technologies, LP
- Quantity
- 25
- Distribution
- US Distribution to the states of : NY, CA, WA, PA, MD, AL, FL and LA.
- Recall date
- August 19, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)