Z-0979-2022Class II

Artis Q.zen ceiling, Model Number 10848354

Name: Z-0979-2022 Artis Q.zen ceiling, Model Number 10848354
Creator: Siemens Medical Solutions USA, Inc
Published: 2022-02-23
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2022-02-23 / Open, Classified / root cause: design

FDA source

Siemens Medical Solutions USA, Inc began a recall of Artis Q.zen ceiling, Model Number 10848354 on 2022-02-23. FDA classified it as Class II and gives the reason as "If the coolant level in the cooling circuit drops below a certain level, this may result in a situation in which the X-ray tube is no longer sufficiently cooled and the system will display the message "TUBE HOT, have a...". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as design.

Recall record

Recall number: Z-0979-2022
Classification: Class II
Status: Open, Classified
Initiated: 2022-02-23
Posted: 2022-04-21
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: Artis Q.zen ceiling, Model Number 10848354
Product code: OWB Interventional Fluoroscopic X-Ray System
Reason for recall: If the coolant level in the cooling circuit drops below a certain level, this may result in a situation in which the X-ray tube is no longer sufficiently cooled and the system will display the message "TUBE HOT, have a break". Several minutes later the system will block X-ray to prevent further damage and display the message "NO XRAY: TUBE TOO HOT".
Root cause tag: design
FDA root cause: Device Design
Action: An URGENT: MEDICAL DEVICE CORRECTION notification letter dated 2/23/22 was sent to customers. Which steps have to be taken by the user to avoid the possible risks associated with this problem? As also described in the Operator Manual, we recommend that the system operator checks the water level of the cooling circuit at least every three months and refills water, if necessary: 1. Open the filling gland of the cooling unit. The water surface must be clearly visible above the cooling ribs. 2. Replenish with water (drinking water quality) if cooling liquid is lacking. Please inform the service technician in case of lacking cooling liquid. How will the corrective action be implemented and what is the efficiency of the corrective actions? The tube cooling unit will be equipped with a water level sensor and the software will be updated accordingly. In case the coolant level drops below a certain threshold the following message will be displayed: Tube cooling water level low: Refill as per Operator Manual . Siemens will correct the error with a hardware and software update via Update Instruction AX002/20/S and AX004/20/S. Our service organization will contact you shortly to arrange a date to perform this corrective action. Please feel free to contact our service organization for an earlier appointment at 1-800-888-7436. We do not consider it necessary to re-examine any patients in relation to the issues described above. Following the correction, the cause is eliminated, and any recurrence of this potential fault is prevented. Acknowledge Receipt of this Safety Advisory Notice Please review, understand, and confirm acknowledgement of the information and instructions outlined in this Urgent Safety Advisory Notice. By signing this document, you are acknowledging that you have read and understand the content therein. If you have received this notification by email via Adobe EchoSign, kindly sign with your digital signature to acknowledge that you have read and understand t
Quantity in commerce: 81 systems
Distribution: US Nationwide.
Product codes and lots: UDI: 4056869010021; Serial Numbers: 111160 111162 111163 111137 111502 111139 111174 111185 111503 111005 111002 111145 111176 111510 111155 111179 111140 111507 111122 111168 111170 111173 111512 111141 111508 111521 111133 111003 111111 111103 111101 111011 111182 111184 111143 111150 111164 111183 111504 111149 111109 111151 111129 111121 111130 111517 111513 111017 111010 111115 111116 111117 111119 111104 111148 111127 111175 111506 111112 111131 111132 111134 111158 111167 111157 111161 111142 111156 111500 111501 111169 111505 111166 111107 111514 111000 111106 111123 111128 111135 Additional Serial Numbers as of 10/4/23: 111125

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0979-2022
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0967-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0968-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0969-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0970-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0971-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0972-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0973-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0974-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0975-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0976-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0977-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0978-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0979-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21
Z-0980-2022	Class II	Ongoing	Voluntary: Firm initiated	2022-04-27	2022-04-21

Product code OWB

K181407Class IIArtis zee/zeego & Artis Q/Q.zenSiemens Medical Solution USA, Inc. / cleared 2018-08-15

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)