FDAClass IIAugust 8, 2018

Discovery IQ 2.0 20cm recall

Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22

Why was Discovery IQ 2.0 20cm recalled?

Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).

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 Number 5432539-22. Serial Number 502674HM5 (System ID Number 510204DISCIQ); Serial Number 504305HM4 (System ID Number 219922PTIQ)

Product
Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22
Recalling firm
GE Healthcare, LLC
Quantity
42 devices total
Distribution
Nationwide distribution to AL, CA, CO, FL, IL, IN, MA, MD, MI, MS, NC, NJ, NY,OH, OK, SC, TN, TX, VA.
Recall date
August 8, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls