FDA Recall Open, Classified

Artis Pheno, Interventional Fluoroscopic X-Ray System, Model No. 10849000

Recall: Z-1294-2022 · Initiated June 10, 2022

Recall

Recall Number
Z-1294-2022
Event Number
90507
Firm
Siemens Medical Solutions USA, Inc
FEI Number
2240869
Product Code
JAA
Status
Open, Classified
Root Cause
Process control
Initiated
June 10, 2022
Posted
June 27, 2022
Address
40 Liberty Blvd, Malvern, PA, 19355-1418

Description

Artis Pheno, Interventional Fluoroscopic X-Ray System, Model No. 10849000

Reason

A video signal from one of the transceivers of the Large Display may be lost. In very rare cases, both transceivers of the Large Display could potentially fail which can lead to the loss of both video signals. This issue can sporadically affect the Large Display in the examination room as well as the displays in the control room.

Action

Firm notified customers of the recall on June 10, 2022 via Urgent Medical Device Correction letters. The firm strongly recommends reinforcing appropriate emergency procedures until the corrective action has been performed. Please ensure that patient treatment can be continued in other ways if there is any possible danger to the safety of the patient. The firm will exchange the affected video transmission links. Their service organization will contact you shortly to arrange a date to perform this corrective action. Please feel free to contact the firm's service organization for an earlier appointment at 1-800-888-7436. The firm does not consider it necessary to re-examine any patients previously treated using the Artis pheno system.

Distribution

Domestic distribution nationwide. Foreign distribution to Australia Austria Belgium Brazil Canada China Colombia Denmark Finland France Germany Hungary Indonesia Iran Italy Japan Kuwait Mexico Monaco Netherlands Norway Poland Singapore Slovakia South Africa Spain Sweden Switzerland Taiwan Thailand Turkey United Arab Emirates United Kingdom United States Vietnam

Quantity

136 systems