Spacelabs Healthcare, Llc: 10 recalls on record

Recalls filed with 1 agency: FDA (10).

First recall on record: June 27, 2012. Most recent: April 2, 2014.

Risk classification: Class II: 10

Most recent recalls

DateAgencyProduct
April 2, 2014FDASpacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11 Rev A and Upda…Z-1273-2014
February 5, 2014FDAARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Model 96281 is intend…Z-0871-2014
November 27, 2013FDASpacelabs Healthcare qube Compact Patient Monitor, Model 91390. It is a patient monitor …Z-0351-2014
November 20, 2013FDASpacelabs Healthcare elance Vital Signs Monitor, Model 93300, with Option S. It is a pat…Z-0188-2014
January 23, 2013FDASpacelabs Smart Disclosure System, Model 92810, is an integrated component of the Intesys…Z-0694-2013
November 28, 2012FDAqube Compact Monitor (Patient Monitor) 91390. The monitor is 26.2 cm x 31.5 cm x 13.2 cm…Z-0403-2013
November 14, 2012FDAThe touchscreen display (model 94267) designed for use with the XPREZZON bedside monitor …Z-0196-2013
September 26, 2012FDAUltraview SL 91493 Integrated Module Housing. PCIS patient monitors is intended to sou…Z-2382-2012
July 25, 2012FDASpacelabs Medical Xprezzon Bedside Monitor, Model 91393, installations with Option C. It …Z-2019-2012
June 27, 2012FDAThe product is Pathfinder SL, version 1.6.0.3057 software used with the Spacelabs Healthc…Z-1831-2012

Questions about this company

How many recalls does Spacelabs Healthcare, Llc have?
Recalert has 10 U.S. recalls on record for Spacelabs Healthcare, Llc, published between June 27, 2012 and April 2, 2014.
What was the most recent Spacelabs Healthcare, Llc recall?
FDA recall Z-1273-2014, published April 2, 2014: Spacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11 Rev A and Update Kit, PN: 040-1565-10. Used for installing ICS G2 Clinical Access software onto hospital personal compute…
Which agencies have handled Spacelabs Healthcare, Llc recalls?
Spacelabs Healthcare, Llc appears as the recalling firm in recalls from: FDA (10).

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