GE Inspection Technologies recall
GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
Why was GE Inspection Technologies recalled?
GE Inspection Technologies, LP ("GE") has discovered that certain of its cabinet x-ray systems may not fully comply with the Food and Drug Administration's (FDA) Cabinet X¿ ray System performance standards, 21 C.F.R. ¿ 1020.40(c)(1)(i)
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?
phoenix micrornelx and nanomelx cabinet x-ray systems
- Product
- GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
- Recalling firm
- GE Inspection Technologies, LP
- Quantity
- 55 US Distribution
- Distribution
- US Distribution to the states of : TX, MD, MI, CA, TN, NH, NY, AL, NC, ID, MA, AZ, IN, FL, PA, NJ, WI, VA, MN, MD CO, GA, SC, OH and DC.
- Recall date
- April 13, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)