—#182369

Product

CARESCAPE ONE, Physiological Patient Monitor - Product Usage: is both a multi-parameter physiological patient monitor and an accessory to a multi-parameter patient monitor intended for use in multiple areas and intra-hospital transport within a professional healthcare facility.

FDA product code: MHX — Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Device class: Class 2
Medical specialty: Cardiovascular
510(k) numbers: K200494
Affected lot / code info: Model: 2087075-001 Serial Numbers: SNA20210164SA, SNA20210031SA, SNA20210045SA, SNA20210064SA, SNA20210319SA, SNA20210330SA, SNA20210348SA, SNA20210361SA, SNA20210362SA, SNA20210375SA, SNA20210376SA, SNA20210377SA, SNA20220003SA, SNA20220005SA, SNA20220007SA, SNA20220018SA, SNA20220022SA, SNA20220026SA, SNA20220045SA, SNA20220047SA, SNA18140024SA, SNA18340072SA, SNA18370025SA, SNA18380001SA, SNA18390009SA, SNA18430002SA, SNA18430059SA, SNA18430088SA, SNA18430116SA, SNA19390023SA, SNA19400056SA, SNA19400143SA, SNA19440048SA, SNA19440069SA, SNA19440071SA, SNA19440122SA, SNA19450008SA, SNA19450025SA, SNA19450128SA, SNA19450136SA, SNA19500072SA, SNA19500073SA, SNA19500080SA, SNA19500084SA, SNA19500086SA, SNA19510001SA, SNA19510005SA, SNA19510007SA, SNA19510012SA, SNA19510027SA, SNA19510053SA, SNA19510055SA, SNA19510103SA, SNA20020119SA, SNA20030070SA, SNA20030071SA, SNA20170022SA, SNA20170080SA, SNA20170082SA, SNA20170112SA, SNA20170113SA, SNA20170116SA, SNA20170117SA, SNA20170118SA, SNA20170120SA, SNA20170131SA, SNA20170134SA, SNA20170136SA, SNA20170139SA, SNA20170145SA, SNA20170160SA, SNA20170161SA, SNA20170164SA, SNA20170166SA, SNA20170168SA, SNA20170169SA, SNA20170171SA, SNA20170173SA, SNA20170176SA, SNA20170181SA, SNA20170182SA, SNA20170194SA, SNA20170197SA, SNA20170198SA, SNA20170232SA, SNA20170237SA, SNA20170264SA, SNA20180002SA, SNA20180008SA, SNA20180009SA, SNA20180011SA, SNA20180012SA, SNA20180017SA, SNA20180018SA, SNA20180023SA, SNA20180025SA, SNA20180026SA, SNA20180027SA, SNA20180028SA, SNA20180029SA, SNA20180030SA, SNA20180031SA, SNA20180032SA, SNA20180040SA, SNA20180042SA, SNA20180043SA, SNA20180044SA, SNA20180071SA, SNA20180073SA, SNA20180074SA, SNA20180075SA, SNA20180076SA, SNA20180080SA, SNA20180096SA, SNA20180101SA, SNA20180102SA, SNA20180109SA, SNA20180117SA, SNA20180144SA, SNA20180161SA, SNA20180162SA, SNA20190321SA, SNA20190331SA, SNA18140004SA, SNA18140005SA, SNA18140007SA, SNA18240025SA, SNA18240026SA, SNA18240030SA, SNA18240032SA, SNA18240044SA, SNA18240051SA, SNA18240054SA, SNA18240079SA, SNA18250010SA, SNA18250012SA, SNA18250017SA, SNA18250023SA, SNA18250026SA, SNA18250033SA, SNA18250034SA, SNA18250036SA, SNA18250044SA, SNA18250061SA, SNA18250072SA, SNA18250075SA, SNA18250078SA, SNA18250080SA, SNA18250081SA, SNA18250082SA, SNA18250086SA, SNA18250092SA, SNA18250093SA, SNA18440051SA, SNA18450094SA, SNA18450098SA, SNA18460013SA, SNA18460040SA, SNA18460072SA, SNA18460075SA, SNA18460083SA, SNA18460086SA, SNA18460089SA, SNA18460101SA, SNA19040008SA, SNA19050016SA, SNA19050025SA, SNA19050028SA, SNA19050030SA, SNA19050031SA, SNA19050033SA, SNA19050038SA, SNA19050043SA, SNA19050044SA, SNA19050045SA, SNA19050046SA, SNA19050049SA, SNA19050050SA, SNA19070071SA, SNA19070072SA, SNA19070073SA, SNA19070074SA, SNA19490074SA, SNA19500037SA, SNA19500043SA, SNA19500054SA, SNA19500059SA, SNA19510003SA, SNA20140029SA, SNA20140031SA, SNA20190324SA, SNA19500131SA, SNA20030120SA, SNA20040052SA, SNA20170179SA, SNA20170195SA, SNA20170203SA, SNA20180054SA, SNA20180057SA, SNA20180059SA, SNA20180077SA, SNA20180100SA, SNA20180103SA, SNA20180104SA, SNA20180113SA, SNA20180115SA, SNA20180142SA, SNA20180145SA, SNA20180146SA, SNA20180147SA, SNA20180154SA, SNA20180158SA, SNA20180163SA, SNA20180168SA, SNA20180183SA, SNA20180202SA, SNA20190024SA, SNA20190026SA, SNA20190030SA, SNA20190034SA, SNA20190038SA, SNA20190056SA, SNA20190057SA, SNA20190059SA, SNA20190060SA, SNA20190063SA, SNA20190106SA, SNA20190107SA, SNA20190109SA, SNA20190112SA, SNA20190114SA, SNA20190115SA, SNA20190116SA, SNA20190117SA, SNA20190119SA, SNA20190120SA, SNA20190121SA, SNA20190122SA, SNA20190124SA, SNA20190126SA, SNA20190127SA, SNA20190130SA, SNA20190131SA, SNA20190132SA, SNA20190133SA, SNA20190134SA, SNA20190137SA, SNA20190141SA, SNA20190142SA, SNA20190143SA, SNA20190144SA, SNA20190145SA, SNA20190146SA, SNA20190147SA, SNA20190148SA, SNA20190149SA, SNA20190152SA, SNA20190153SA, SNA20190155SA, SNA20190156SA, SNA20190159SA, SNA20190161SA, SNA20190174SA, SNA20190201SA, SNA20190204SA, SNA20190206SA, SNA20190209SA, SNA20190210SA, SNA20190214SA, SNA20190216SA, SNA20190217SA, SNA20190218SA, SNA20190219SA, SNA20190220SA, SNA20190221SA, SNA20190222SA, SNA20190223SA, SNA20190229SA, SNA20190230SA, SNA20190231SA, SNA20190232SA, SNA20190233SA, SNA20190235SA, SNA20190236SA, SNA20190237SA, SNA20190238SA, SNA20190239SA, SNA20190240SA, SNA20190247SA, SNA20190279SA, SNA20190289SA, SNA20190328SA, SNA20190339SA, SNA20200031SA, SNA20200081SA, SNA20200403SA.

Why it was recalled

CARESCAPE ONE may not provide visual and audible alarms for Ventricular Fibrillation (V Fib), if V Fib occurs at the time CARESCAPE ONE is docked to a CARESCAPE B450/B650/B850 host monitor.

Root cause (FDA determination)

Software Design Change

Action the firm took

You can continue to use your CARESCAPE ONE to monitor patients. Follow the instructions below each time the CARESCAPE ONE is docked to a CARESCAPE B450/B650/B850 host monitor. 1. As per the User Manual, closely observe and monitor the patients clinical condition and ECG waveforms on the CARESCAPE B450/B650/B850 host monitor for V Fib during the Learning phase and for several minutes after the Learning phase to allow the algorithm to reach optimal detection performance. 2. As per the User Manual, if the Learning message on the host monitor does not clear after 30 seconds, select the Relearn QRS option from the ECG menu on the host monitor following these steps. Select the HR parameter window. Select Advanced > Page 1. Select Relearn QRS. GE Healthcare will correct all affected products at no cost to you. A GE Healthcare representative will contact you to arrange for the correction. After the CARESCAPE ONE Monitor has been updated, discontinue usage of any previous versions of CARESCAPE ONE software. Destroy any software media containing previous versions of CARESCAPE ONE software, including reimage, upgrade kits, and FRUs. If you have any questions or concerns regarding this notification, please contact GE Healthcare Service at 1-800-437-1171 or your local Service Representative.

Recalling firm

Firm: GE Healthcare, LLC
Address: 3000 N Grandview Blvd, Waukesha, Wisconsin 53188-1615

Distribution

Distribution pattern: Worldwide distribution - US Nationwide distribution including in the states of MT, NC, TX and WI. The countries of Australia, Austria, Bahrain,Belgium, Bolivia, Brazil ,Canada, Chile, Check Republic, Denmark, Ecuador, Egypt, Estonia, Finland, France, French Guiana, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Ireland, Israel, Italy, Japan, Kenya, Korea, Kuwait, Latvia, Lebanon, Lithuania, Macedonia, Malaysia, Malta, Morocco, Netherlands, New Zealand, Norway, Oman, Pakistan, Panama, Philippines, Poland, Portugal, Qatar, Republic of Serbia, Russia, Saudi Arabia, Singapore, Saint Martin, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Thailand, United Arab Emirates, United Kingdom.

Timeline

Recall initiated: 2020-06-22
Posted by FDA: 2020-08-04
Terminated: 2024-08-19
Status: —

Source: openFDA Device Recall endpoint. Recall record ID #182369. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.