FDAClass IISeptember 4, 2019

Somatom Go.up recall

SOMATOM go.Up; Models #11061620 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients…

Why was Somatom Go.up recalled?

The injector holder could potentially fall off together with the injector and the storage box.

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?

Serial Number 111232 111409 111332 111370 111371 111383 111378 111352 111299 111273 111373 111289 111339 111317 111333 111297 111237 111303

Product
SOMATOM go.Up; Models #11061620 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients…
Recalling firm
Siemens Medical Solutions USA, Inc
Quantity
18 units
Distribution
US Nationwide Distribution in the states FL KS WI NE MS OH TX NY LA IN IL OK MI GA NJ AK CT AL MD
Recall date
September 4, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls