SOMATOM go.Now recall
SOMATOM go.Now (Model #11061620), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is…
Why was SOMATOM go.Now recalled?
The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. This may cause a delay in diagnosis or patient scans.
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: 111379 111374 111307 111225 111313 111350 111306 111281 111323 111219 111232 111271 111351 111369 111332 111370 111266 111371 111355 111310 111308 111328 111345 111310 111319 111286 111378 111338 111236 111352 111324 111344 111233 111368 111366 111230 111299 111315 111273 111249 111373 111289 111250 111317 111333 111297 111237 111341 111367 111303 111293 111302 111277
- Product
- SOMATOM go.Now (Model #11061620), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is…
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 53
- Distribution
- US Nationwide distributed in the states of AK, AL, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NY, OH, PA, SC, TX, VA, WA, WI, and Puerto Rico.
- Recall date
- July 10, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)