Z-2902-2011

Ultraview Spacelabs Medical Multigas Analyzer, Model 91518, V1.00.14. Spacelabs Healthcare Llc. Monitors gas...

Name: Z-2902-2011 Ultraview Spacelabs Medical Multigas Analyzer, Model 91518, V1.00.14. Spacelabs Healthcare Llc. Monitors gas...
Creator: Spacelabs Healthcare, Llc
Published: 2011-06-08
License: https://open.fda.gov/license/

GE Healthcare / initiated 2011-06-08 / Terminated / root cause: software

FDA source

Spacelabs Healthcare, Llc began a recall of Ultraview Spacelabs Medical Multigas Analyzer, Model 91518, V1.00.14. Spacelabs Healthcare Llc. Monitors gas concentrations and alerts clinical personnel when... on 2011-06-08. The reason FDA records is "Spacelabs received a report of the Model 91518 Multigas Analyzer trending low levels of an anesthetic agent that is not present during a particular case. The error is limited to only the trend table data". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as software.

Recall record

Recall number: Z-2902-2011
Status: Terminated
Initiated: 2011-06-08
Posted: 2011-08-01
Terminated: 2011-09-21
Recalling firm: GE Healthcare
Product: Ultraview Spacelabs Medical Multigas Analyzer, Model 91518, V1.00.14. Spacelabs Healthcare Llc. Monitors gas concentrations and alerts clinical personnel when the concentration of anesthetic agents, oxygen, carbon dioxide, or nitrous oxide falls outside of defined limits. The anesthetic agent being administered is automatically identified.
Product code: CBR Analyzer, Gas, Nitrous-Oxide, Gaseous Phase (Anesthetic Conc.)
Reason for recall: Spacelabs received a report of the Model 91518 Multigas Analyzer trending low levels of an anesthetic agent that is not present during a particular case. The error is limited to only the trend table data.
Root cause tag: software
FDA root cause: Software design
Action: Spacelabs Healthcare, Llc. sent a "Customer Bulletin" dated June 20, 2011 to all affected customers. The customers were notified of the trend problem and are advised to follow the instructions in the Perioperative section and the ADMIT/DISCHARGE section of the users manual. For questions contact Spacelabs Healthcare at 1-800-522-7025 and select 2 for Technical Support or 1-425-657-7200 x5089.
Quantity in commerce: 481 units worldwide (333 units internationally and 148 units in the US)
Distribution: Worldwide Distribution: (USA) Nationwide distribution, and the countries of ARGENTINA, BAHRAIN, BOLIVIA, CANADA, CHILE, CHINA, COLOMBIA, CZECH REPUBLIC, ECUADOR, EGYPT, FRANCE, INDIA, MEXICO, NICARAGUA, PARAGUAY, PERU, POLAND, Slovakia, SWITZERLAND, SYRIAN ARAB REPUBLIC, TAIWAN, CHINA, THAILAND, UNITED ARAB EMIRATES, U.K., URUGUAY, VENEZUELA, and VIETNAM.
Product codes and lots: Model 91518, V1.00.14. Serial Numbers: 1518-000003, 1518-000008, 1518-000013, 1518-000014, 1518-000016, 1518-000024, 1518-000029, 1518-000036, 1518-000040, 1518-000044, 1518-000226, 1518-000228, 1518-000231, 1518-000233, 1518-000243, 1518-000349, 1518-000354, 1518-000355, 1518-000389, 1518-000399, 1518-000457, 1518-000752, 1518-000819, 1518-000825, 1518-000846, 1518-000948, 1518-000991, 1518-001341, 1518-001393, 1518-001394, 1518-001395, 1518-001522, 1518-001536, 1518-001654, 1518-001655, 1518-001708, 1518-001734, 1518-001736, 1518-001853, 1518-001972, 1518-002065, 1518-002089, 1518-002097, 1518-002114, 1518-002116, 1518-002117, 1518-002118, 1518-002119, 1518-002120, 1518-002121, 1518-002122, 1518-002123, 1518-002124, 1518-002125, 1518-002126, 1518-002127, 1518-002128, 1518-002129, 1518-002130, 1518-002131, 1518-002132, 1518-002133, 1518-002134, 1518-002135, 1518-002136, 1518-002137, 1518-002138, 1518-002139, 1518-002140, 1518-002141, 1518-002142, 1518-002143, 1518-002144, 1518-002145, 1518-002146, 1518-002147, 1518-002148, 1518-002149, 1518-002150, 1518-002151, 1518-002152, 1518-002153, 1518-002154, 1518-002155, 1518-002156, 1518-002157, 1518-002161, 1518-002162, 1518-002163, 1518-002164, 1518-002166, 1518-002167, 1518-002168, 1518-002169, 1518-002170, 1518-002171, 1518-002172, 1518-002173, 1518-002174, 1518-002175, 1518-002176, 1518-002177, 1518-002178, 1518-002179, 1518-002180, 1518-002181, 1518-002182, 1518-002183, 1518-002184, 1518-002185, 1518-002186, 1518-002187, 1518-002188, 1518-002190, 1518-002191, 1518-002192, 1518-002205, 1518-002206, 1518-002207, 1518-002208, 1518-002209, 1518-002210, 1518-002211, 1518-002212, 1518-002213, 1518-002214, 1518-002215, 1518-002216, 1518-002217, 1518-002218, 1518-002219, 1518-002220, 1518-002221, 1518-002222, 1518-002223, 1518-002224, 1518-002225, 1518-002226, 1518-002227, 1518-002228, 1518-002229, 1518-002230, 1518-002231, 1518-002232, 1518-002233, 1518-002234, 1518-002235, 1518-002236, 1518-002237, 1518-002238, 1518-002239, 1518-002240, 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Product code CBR

K053599Class IISpacelabs Medical Multigas Analyzer Module 91518 and AccessoriesSpacelabs Medical, Inc. / cleared 2006-04-19

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 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)