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U.S. Department of Health and Human Services

Class 1 Device Recall Philips Respironics Trilogy 100, Trilogy 200, Trilogy 202

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  Class 1 Device Recall Philips Respironics Trilogy 100, Trilogy 200, Trilogy 202 see related information
Date Initiated by Firm February 11, 2014
Date Posted March 06, 2014
Recall Status1 Terminated 3 on April 17, 2015
Recall Number Z-1143-2014
Recall Event ID 67550
510(K)Number K083526  K093416  K093905  
Product Classification Ventilator, continuous, facility use - Product Code CBK
Product Trilogy Ventilators
The Respironics Trilogy 100 system provides continuous or intermittent ventilator support for the care of individuals who require mechanical ventilation. Trilogy 100 is intended for pediatric through adult patients weighing at least 5 kg (11 lbs.). The device is intended to be used in home, institution/hospital, and portable applications such as wheelchairs and gurneys, and may be used for both invasive and non-invasive ventilation. It is not intended to be used as a transport ventilator. Trilogy 200 Intended Use: The Respironics Trilogy 200 system provides continuous or intermittent ventilator support for the care of individuals who require mechanical ventilation. Trilogy 200 is intended for pediatric through adult patients weighing at least 5 kg (11 lbs.). The device is intended to be used in home, institution/hospital, and portable applications such as wheelchairs and gurneys, and may be used for both invasive and non-invasive ventilation. Trilogy 202 Intended Use: The Respironics Trilogy 202 system provides continuous or intermittent ventilator support for the care of individuals who require mechanical ventilation with or without air/oxygen blending. Trilogy 202 is intended for pediatric through adult patients weighing at least 5 kg (11 lbs.). The device is intended to be used in hospitals and institutions, and for portable applications such as wheelchairs and gurneys only when in an institutional setting. It may be used for both invasive and non-invasive ventilation. It is not intended to be used as a transport ventilator.
Code Information Model (s), Catelogue, or Code Numbers were identified as: 1040000 Trilogy 202 International, Number 1040005 Trilogy200 USA, 1054096 Trilogy 100 International,  1054260 Trilogy 100 USA, 1040004 Trilogy 02, and 1058180 Garbin. Multiple serial numbers also indicated: TV114011447; TV114011448; TV114011449 TV11401144A; TV11401144B; TV11401144C; TV11401144D; TV11401144E; TV114011450; TV114011451; TV11401145B; TV11401145C; TV11401145D; TV11401145F; TV114011460; TV114011461; TV114011462; TV114011464;  TV114012326; TV114012364;TV1140120A9; TV114012323; TV11401212C; TV11401230F; TV11401235A; TV11401235C; TV114012370TV114012371 TV114012372; TV114012376; TV114012415; TV114012465; TV21401150C; TV214011510; TV11401153D; TV11401213E; TV21401150F;TV114012165; TV11401133A;TV114012318; TV114012433; TV11401223A; TV11401223E; TV114012170; TV114011722; TV1140120B2;TV114012416; TV114012235; TV114012148; TV114011550; TV1140120BB; TV114012469; TV114012459; TV114012732;TV21401150A; TV11401130C; TV11401236D; TV114011455 ; TV114011465; TV114012239;TV11401223B; TV11401224D;TV114011336 TV11401133B;TV21401150E;TV214011511;TV214011513;TV214011515; TV214011516;TV214011519;TV21401151B;TV21401151F;TV21401210B TV214012117;TV214012119;TV21401211A;TV21401211D;TV214012122; TV114011712;TV114011458; TV114012133;TV114012361; TV114012429 TV11401245B TV114011724 TV114011727 TV114011740 TV214011512 TV21401210C TV214012111 TV214012120 TV214012121 TV21401240D TV114012333 TV11401233E TV114012349 TV11401234C TV114012422 TV11401243B TV11401245F TV11401231C TV114012355 TV114012137 TV11401233C TV1140120DB TV114012453 TV114011635 TV114011752 TV11401134F TV114011741 TV114011757 TV114012095 TV1140120CD TV1140120E3 TV11401215B TV114012130 TV114012134 TV114012343 TV114012347 TV114012462 TV114012473 TV114011554 TV114011711 TV114011719 TV114011723 TV114011725 TV114012259 TV014011405 TV014011503 TV014011504 TV21401210D TV21401210F TV214012114 TV214012116 TV11401207D TV11401207F TV114012085 TV11401208C TV1140120A6 TV114011311 TV1140120C1 TV114012146 TV1140120E2 TV11401174E TV114011754 TV1140120DA TV11401233A TV114012342 TV11401234B TV11401241D TV114012441 TV114012456 TV114012458 TV11401245A TV11401245C TV11401245D TV014012302 TV014012404 TV014012204 TV014012206 TV014012207 TV014012208 TV014012402 TV014012405 TV014012406 TV014012407 TV014012408 TV014011601 TV014011607 TV21401151D TV214011522 TV114011335 TV114012313 TV11401236C TV114011744 TV114012090 TV11401209C TV11401209F TV114012098 TV11401230C TV114012377 TV11401213B TV11401214A TV114012154 TV11401245E TV11401230B TV114012414 TV114012417 TV014011401 TV014011406 TV11401214D TV11401246D TV114012418 TV11401241C TV11312282C TV11401130F TV11401146A TV11401146C TV11401146F TV114011523 TV114011524 TV11401152A TV11401152D TV114011530 TV114011536 TV114011538 TV11401155C TV11401170F TV114011717 TV11401172C TV1140120DC TV114012160 TV114012163 TV11401216A TV11401216B TV114012240 TV114012446 TV11401246E TV1140120D4 TV1140120D5 TV114012155 TV114012157 TV114012423 TV114012132 TV11401241E TV114012432 TV11401212E TV114012312 TV11401231D TV114012351 TV11401235D TV114012468 TV11401246F TV114012470 TV114012472 TV11401241A TV11401242A TV1140120D0 TV11401224E TV114012233  TV114012234 TV114012237 TV11401223F TV11401224C TV114012250 TV114012255 TV114012256 TV11401225B TV114011746 TV114012322 TV11401154F TV11401231A TV114012330 TV114011317 TV11401152C TV114011540 TV114011546 TV11401154A TV11401154E TV114011551 TV114011555 TV114011562 TV11401170D TV114011718 TV11401172B TV114011745 TV114011760 TV21401151A TV21401151C TV1140120D9 TV114012162 TV114012238 TV114012242 TV11401224B TV114012358 TV11401161A TV11401161F TV114011623 TV11401162E TV11401162F;   
Recalling Firm/
Manufacturer		 Phillips Respironics, Inc.
1001 Murry Ridge Ln
Murrysville PA 15668-8517
For Additional Information Contact Customer Support
724-733-0200
Manufacturer Reason
for Recall		 Internal testing revealed a potentially defective component on the power management board that could affect the function of certain Trilogy Ventilators resulting in loss of therapy to patients.
FDA Determined
Cause 2		 Component design/selection
Action Philips sent an Urgent - Medical Device Recall letter on February 11, 2014, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to review the information contained in the Notice with all members of their staff who need to be aware of the contents of the communication. For further information or support concerning the issue, customers were instructed to contact Philips Respironics at 877-387-3311. For questions regarding this recall call 724-733-0200.
Quantity in Commerce 572
Distribution Worldwide Distribution - USA (nationwide) and the countries of France, Great Britian, China, India, Italy, Korea, Kuwait, Nehterlands, and Singapore.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = CBK and Original Applicant = RESPIRONICS INC., SLEEP & HOME RESPIRATORY GROUP
510(K)s with Product Code = CBK and Original Applicant = RESPIRONICS, INC.
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