FDA Device Recalls

Recalls /

#168354

Product

Touchscreen display kit. Sold under the following product names: TOUCHSCREEN DISPLAY KIT 11.X ENGLISH FOR USA, TOUCHSCREEN DISPLAY KIT 11.X ENGLISH, TOUCHSCREEN DISPLAY KIT 11.X GERMAN, TOUCHSCREEN DISPLAY KIT 11.X DUTCH, TOUCHSCREEN DISPLAY KIT 11.X FRENCH, TOUCHSCREEN DISPLAY KIT 11.X DANISH, TOUCHSCREEN DISPLAY KIT 11.X ESTONIAN, TOUCHSCREEN DISPLAY KIT 11.X ITALIAN, TOUCHSCREEN DISPLAY KIT 11.X NORWEGIAN. Product Usage: The GE Datex-Ohmeda Aisys Anesthesia System is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric, adult). The device is intended for volume or pressure control ventilation. The Aisys is not suitable for use in a MRI environment.

FDA product code
BSZGas-Machine, Anesthesia
Device class
Class 2
Medical specialty
Anesthesiology
510(k) numbers
K110213, K170872
Affected lot / code info
Model Number, UDI Number, (Serial Number):  2097673-001-US (4651698-1); 2097673-001-US (4651698-3); 2097673-001-US (4651698-4); 2097673-001-US (4651726-1); 2097673-001-US (4652206-1); 2097673-001-US (4652206-2); 2097673-001-US (4649618-1); 2097673-001-US (4649618-2); 2097673-001-US (4649618-3); 2097673-001-US (4649618-4); 2097673-001-US (4649618-5); 2097673-001-US (4653227-1); 2097673-001-US (4653227-2); 2097673-001-US (4653227-3); 2097673-001-US (5474296-1); 2097673-001-US (4652587-1); 2097673-001-US (4652587-2); 2097673-001-US (4652587-3); 2097673-001-US (4652587-4); 2097673-001-US (4652587-5); 2097673-001-US (4652587-6); 2097673-001-US (4632861-1); 2097673-001-US (4632861-2); 2097673-001-US (4632861-3); 2097673-001-US (4644953-1); 2097673-001 (5463757-1); 2097673-001 (5467309-16); 2097673-001 (5471699-1); 2097673-001 (5471699-2); 2097673-001 (5471699-3); 2097673-001 (5475515-1); 2097673-001 (5475515-2); 2097673-001 (5475516-1); 2097673-001 (5475516-10); 2097673-001 (5475516-2); 2097673-001 (5475516-3); 2097673-001 (5475516-4); 2097673-001 (5475516-5); 2097673-001 (5475516-6); 2097673-001 (5475516-7); 2097673-001 (5475516-8); 2097673-001 (5475516-9); 2097673-001 (5475528-1); 2097673-001 (5475528-10); 2097673-001 (5475528-11); 2097673-001 (5475528-12); 2097673-001 (5475528-13); 2097673-001 (5475528-14); 2097673-001 (5475528-15); 2097673-001 (5475528-16); 2097673-001 (5475528-17); 2097673-001 (5475528-18); 097673-001 (5475528-19); 2097673-001 (5475528-2); 2097673-001 (5475528-3); 2097673-001 (5475528-4); 2097673-001 (5475528-5); 2097673-001 (5475528-6); 2097673-001 (5475528-7); 2097673-001 (5475528-8); 2097673-001 (5475528-9); 2097673-001 (5481650-1); 2097673-001 (5481650-10); 2097673-001 (5481650-2); 2097673-001 (5481650-3); 097673-001 (5481650-4); 2097673-001 (5481650-5); 2097673-001 (5481650-6); 2097673-001 (5481650-7); 2097673-001 (5481650-8); 2097673-001 (5481650-9); 2097673-001 (5471701-1); 2097673-001 (5471701-2); 2097673-001 (5471702-1); 2097673-001 (5472013-1); 2097673-001 (5472013-10); 097673-001 (5472013-12); 2097673-001 (5472013-14); 2097673-001 (5472013-15); 2097673-001 (5472013-16); 2097673-001 (5472013-17); 2097673-001 (5472013-18); 2097673-001 (5472013-3); 2097673-001 (5472013-4); 2097673-001 (5472013-5); 2097673-001 (5472013-6); 2097673-001 (5472013-7); 2097673-001 (5472013-8); 2097673-001 (5463631-1); 2097673-001 (5463631-2); 2097673-001 (5466892-1); 2097673-001 (5466892-10); 2097673-001 (5466892-2); 2097673-001 (5466892-3); 2097673-001 (5466892-4); 2097673-001 (5466892-5); 2097673-001 (5466892-6); 2097673-001 (5466892-7); 2097673-001 (5466892-8); 2097673-001 (5466892-9); 2097673-DE (5480919-1); 2097673-NL (5473301-1); 2097673-NL (5473301-2); 2097673-NL (5473301-3); 2097673-NL (5473301-4); 2097673-NL (5473301-5); 2097673-NL (5473301-6); 2097673-FR (5481162-1); 2097673-NL (5481369-1); 2097673-NL (5481369-2); 2097673-NL (5481369-3); 2097673-NL (5481369-4); 2097673-NL (5481369-5); 2097673-NL (5481369-6); 2097673-NL (5481369-7); 2097673-NL (5481369-8); 2097673-NL (5481369-9); 2097673-001 (5462738-1); 2097673-001 (5462738-2); 2097673-FR (5475371-1); 2097673-FR (5475371-2); 2097673-FR (5475371-3); 2097673-FR (5475371-4); 2097673-FR (5475371-5); 2097673-FR (5479900-1); 2097673-DA (5453900-1); 2097673-ET (5461749-1); 2097673-FR (5481462-1); 2097673-FR (5481462-2); 2097673-FR (5481462-3); 2097673-FR (5481462-4); 2097673-FR (5481462-5); 2097673-FR (5481462-6); 2097673-FR (5481462-7); 2097673-FR (5481462-8); 2097673-FR (5481462-9); 2097673-FR (5473743-1); 2097673-FR (5473743-2); 2097673-FR (5473743-3); 2097673-FR (5473743-4); 2097673-FR (5473743-5); 2097673-FR (5473744-1); 2097673-FR (5473744-2); 2097673-FR (5473744-3); 2097673-FR (5473744-4); 2097673-FR (5473744-5); 2097673-FR (5473744-6); 2097673-FR (5458277-1); 2097673-FR (5458277-2); 2097673-001 (5455478-1); 2097673-IT (5476554-1); 2097673-IT (5476554-2); 2097673-IT (5476554-3); 2097673-NL (5450447-1); 2097673-NL (5450447-3); 2097673-NL (5450447-5); 2097673-NL (5450447-6); 2097673-NO (5474251-1); 2097673-001 (5476468-70); 2097673-001 (5476468-71); 2097673-001 (5476468-72); 2097673-001 (5476468-73); 2097673-001 (5476468-74); 2097673-001 (5476468-75); 2097673-001 (5476468-76); 2097673-001 (5476468-77); 2097673-001 (5476468-78); 2097673-001 (5476468-79); 2097673-001 (5476468-80); 2097673-001 (5476468-81); 2097673-001 (5476468-82); 2097673-001 (5476468-83); 2097673-001 (5476468-84); 2097673-001 (5476468-85); 2097673-001 (5476468-86); 2097673-001-US (4673852-1); 2097673-001-US (4673852-2); 2097673-001-US (4673852-3);   Additional Serial Numbers - Model Number, UDI Number, (Serial Number): 2097673-001-US, Not Applicable, (ANAM00306);  2097673-001-US, Not Applicable, (ANAP00354);  2097673-001-US, Not Applicable, (APWU00297);  2097673-001-US, Not Applicable, (ANAP00715);  2097673-001-US, Not Applicable, (ANAR00602);  2097673-001-US, Not Applicable, (ANAR00603);  2097673-001-US, Not Applicable, (ANAN00169);  2097673-001-US, Not Applicable, (ANAP00574);  2097673-001-US, Not Applicable, (ANAP00575);  2097673-001-US, Not Applicable, (ANAP00576);  2097673-001-US, Not Applicable, (ANAP00577);  2097673-001-US, Not Applicable, (ANAQ01175);  2097673-001-US, Not Applicable, (ANAP00172);  2097673-001-US, Not Applicable, (ANAP00861);  2097673-001-US, Not Applicable, (ANAP00870);  2097673-001-US, Not Applicable, (ANAP00872);  2097673-001-US, Not Applicable, (ANAS00398 );  2097673-001-US, Not Applicable, (ANAL00105);  2097673-001-US, Not Applicable, (ANAL00106);  2097673-001-US, Not Applicable, (ANAL00107);  2097673-001-US, Not Applicable, (ANAL00108);  2097673-001-US, Not Applicable, (ANAL00109);  2097673-001-US, Not Applicable, (ANAL00116);  2097673-001-US, Not Applicable, (ANAM00439);  2097673-001-US, Not Applicable, (ANAM00440);  2097673-001-US, Not Applicable, (ANAM00441);  2097673-001-US, Not Applicable, (ANAP01088);  2097673-001-US, Not Applicable, (ANAP01090);  2097673-001-US, Not Applicable, (ANAP01091);  2097673-001, Not Applicable, (ANAN00604);  2097673-001, Not Applicable, (ANAM01165);  2097673-001, Not Applicable, (ANAM01158);  2097673-001, Not Applicable, (ANAM00815);  2097673-001, Not Applicable, (ANAM00816);  2097673-001, Not Applicable, (ANAM00817);  2097673-001, Not Applicable, (ANAM00818);  2097673-001, Not Applicable, (ANAM00819);  2097673-001, Not Applicable, (ANAM00820);  2097673-001, Not Applicable, (ANAM00821);  2097673-001, Not Applicable, (ANAM00822);  2097673-001, Not Applicable, (ANAM00823);  2097673-001, Not Applicable, (ANAM00824);  2097673-DE, Not Applicable, (ANAP01156);  2097673-001, Not Applicable, (ANAR00318);  2097673-001, Not Applicable, (ANAR00319);  2097673-FR, Not Applicable, (ANAR05232);  2097673-FR, Not Applicable, (ANAR05233);  2097673-FR, Not Applicable, (ANAR05234);  2097673-FR, Not Applicable, (ANAR05235);  2097673-FR, Not Applicable, (ANAR05236);  2097673-FR, Not Applicable, (ANAP01419);  1011-9000-000, Not Applicable, (APWT00661);  1011-9000-000, Not Applicable, (APWT00662);  1011-9000-000, Not Applicable, (APWT00664);  1011-9000-000, Not Applicable, (ANAN00664);  1011-9000-000, Not Applicable, (ANAN00666);  1011-9000-000, Not Applicable, (ANAN00667);  1011-9000-000, Not Applicable, (ANAN00669);  1011-9000-000, Not Applicable, (ANAN00670);  1011-9000-000, Not Applicable, (ANAN00671);  1011-9000-000, Not Applicable, (ANAN00890);  1011-9000-000, Not Applicable, (ANAN00891);  1011-9000-000, Not Applicable, (ANAR00396);  1011-9000-000, Not Applicable, (APWT02012);  1011-9000-000, Not Applicable, (APWT02013);  1011-9000-000, Not Applicable, (ANAN01101);  1011-9000-000, Not Applicable, (ANAP00605);  2097673-FR, Not Applicable, (ANAQ00803);  2097673-FR, Not Applicable, (ANAQ00806);  2097673-FR, Not Applicable.(ANAQ00948);  2097673-FR, Not Applicable, (ANAR05145);  2097673-FR, Not Applicable, (ANAR05150);  2097673-FR, Not Applicable, (ANAR05513);  2097673-FR, Not Applicable, (ANAR05517);  2097673-FR, Not Applicable, (ANAS00665);  2097673-FR, Not Applicable, (ANAS00666);  2097673-FR, Not Applicable, (ANAS00668);  2097673-FR, Not Applicable, (ANAS00971);  2097673-NO, Not Applicable, (ANAQ01098);

Why it was recalled

Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with PSVPro Spontaneous Breathing Modes do not provide the PSVPro ventilation mode feature of transitioning to SIMV PCV backup ventilation mode. PSVPro Spontaneous Breathing Modes do not provide the feature of transitioning to SIMV PCV backup ventilation mode for a patient who stops spontaneous breathing if the PSVPro ventilation mode is in use prior to the clinician starting the Cycling Procedure.

Root cause (FDA determination)

Software design

Action the firm took

GE Healthcare notified customers on about 09/27/2018 via "URGENT MEDICAL DEVICE CORRECTION" letter. The letter informed customers that they could continue to use the anesthesia device. The issue can only occur if the patient stops spontaneous breathing in PSVPro ventilation mode after completion of lung recruitment breaths. Stopping the Cycling Procedure resolves the issue. Continue to monitor patient as is normal for Apnea. A GE Healthcare representative will contact each customer to arrange for the correction. Questions or concerns can be directed to 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 in the states of CA, CO, DC, FL, GA, HI, IA, IL, IN, KY, LA, ,MA, MD, MI, MN, MO, MT, NC, NE, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV. Countries of Argentina, Australia, Austria, Belgium, Bolivia, Brazil, Canada, China, Colombia, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Iceland, India, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea (Republic of), Kuwait, Macedonia, Mexico, Netherlands, New Zealand, Nigeria, Norway, Peru, Portugal, Qatar, Russia, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, Vietnam.

Timeline

Recall initiated
2018-09-27
Posted by FDA
2018-11-09
Terminated
2021-04-12
Status

Source: openFDA Device Recall endpoint. Recall record ID #168354. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.