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Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is a device that displays medical ima...

FDA Device Recall #Z-2503-2021 — Class II — August 6, 2021

Recall Summary

Recall Number Z-2503-2021
Classification Class II — Moderate risk
Date Initiated August 6, 2021
Status Ongoing
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm GE Healthcare, LLC
Location Waukesha, WI
Product Type Devices
Quantity 462 (279 US; 183 OUS)

Product Description

Centricity Universal Viewer and Viewer 6.0 - Product Usage: Is a device that displays medical images (including mammograms) and data from various imaging sources. Includes the following Model Numbers: 1. Model Number: 2090255-001; 2. Model Number: 2088026-723; 3. Model Number: 2102676-001; 4. Model Number: 2104867-044.

Reason for Recall

Image acquisition failures and synchronization failure with the Centricity Enterprise Archive

Distribution Pattern

AK, AZ, CA, CO, DE, FL, GA, IA, IN, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NJ, NM, NV, NY, OH, OK, OR, PA, SD, TX, UT, WA, WI, WV and WY. Austria, Brazil, Canada, France, Germany, Ghana, India, Ireland, Israel, Italy, Kuwait, Netherlands, Panama, Poland, Russia, Saudi Arabia, Slovenia, South Africa, Spain, Switzerland, Turkey, United Kingdom and Uruguay.

Lot / Code Information

1. Model Number: 2090255-001 (Centricity Universal Viewer with PACS-IW foundation software versions 6.0 through 6.0 SP7.1) System ID (UDI-DI if applicable): PMIO14194768, PMIO20084199, PACS-IW-231, CITRUSVAL20884363, CITRUSVAL20884364, CITRUSVAL20884365, PACS-IW-155, PRIMEHEAL02315681, PRIMEHEAL20501355, PARKVIEWC21200827 (840682103800), PARKVIEWC21200830 (840682103800), PACS-IWUVN2-441, QUEEN19630914, QUEEN19630915, QUEEN19630916T, QUEEN20553950, 203268UVSW, DELAWAREC01589220, PACS-IW-462UV, PACS-IW-462UVN1, PACS-IW-126, PACS-IW-1062, OFMC01819402, OFMC20791988, HGS01766912, HGS20584004 (840682103800), GA001PACTRL01, TRGI02180958, DRY01810490, DRY19670358, PACS-IW-101, RML20502096, PACS-IWUV-239, PACS-IW-00813, PHS01374810, 01722652SEAS, 02031921SEASN1, MARYLANDF17985489, MYRTLEHIL17713895, MYRTLEHIL01444483, MYRTLEHIL17713895, VT01766830, VT01977629, PACS-IW-2637, SRMC01982629, PACS-IWUV-568, 1-142022244, PACS-IWUV-1131, OGAA02373799NOD1, ALLG00558571 (840682103800), EXC02189547, EXC01584099, PACS-IW-574, PRIME HEAL19508102, PRIME HEAL19050922, PRIME HEAL19050921, PACS-IW-219, ANCL00558570, ANCL02157634, NSW01452088, NSW20080545, MARYLANDF17985489, PACS-IW-518UV (840682103800), MTGD02393053, MTGD00558454, PACS-IW-44, QUENTIN01970717, LAKESIDEM02256808, BMC12P00558644P1, BMC12T02267839, BMC12N01271417N1, PACS-IW-58, SMCO02039946PC (840682103800), BWH01301357, PACS-IW-349, PACS-IW-255, 1-357059471, CAROCOMMU02205222, CAROCOMMU01459013, CSPA01291589 (840682103800), CSPA02097167 (840682103800), PACS-IW-79, PACS-IW-93, 1-276423210, MFCI01448329, LSFH02032334, CORONAREG01300927, 951737IWUWWN1, CORONAREG02288447, 1-382753509, CITRUSVAL19618406, MGMC02288391, MGMC02398531, 1-473998727, BARRETTHO00558704, BARRETTHO17737529, FORTDUNCA01298556 (840682103800), FORTDUNCA02395799 (840682103800), 1-283597082, TTU01973509, AVHL02396030, PACS-IW-511, PACSIWTEST, PACS-IW-386UV (840682103800), PACS-IW-486-UV (840682103800), PACS-IW-486-UVN1 (840682103800), PACS-IW-390 (840682103800), PACS-IW-202TEST, PACS-IW-202, HZC14961014, AVHL02396026, AVHL02396027, AVHL02396028, AVHL02396029, PACS-IW-419, PMRM14768587UVProxy, HANNIBALR02179353 (840682103800), TESTHANNIBALR02255613 (840682103800), HANN16174584UVProxy (840682103800), PACS-IW-189 (840682103800), HARTSDALE14768195 (840682103800), HOA01451973 (840682103800), RML01448365 (840682103800), ICA01367198 (840682103800), ICA14776604 (840682103800), JKS01452133 (840682103800), JKS14776447UVSFNode (840682103800), JKS14776448UVProxy (840682103800), JKS14776449UVTest (840682103800), PACS-IW-181, GTEC01477448, GTEC01477447, GTEC15993728UVProxy3, 1-592001096 (840682103800), UHSD14767800 (840682103800), PACS-IW-551UVN1 (840682103800), PACS-IW-551UVN2 (840682103800), UV1-154550926, DHOL19603374, DHOL19603375, PACS-IW-551UV (840682103800), PACS-IW-424CTLR, PACS-IW-424UVN1, PACS-IW-424UVN2, SFCS19667347, SFCS15961473, SFCS15961473, MHOG01806096, PACS-IW-166, PACS-IW-166T, MCT02277843, MCT02278145, PACS-IW-565, PACS-IWT-565, WGH00558334CTRL, WGH02372377PROX, WGH02372375BACK, 1-464783615, PACS-IW-389, BVH00558643, PACS-IW-348UV (840682103800), NRVM19609993UVT (840682103800), NRVM19611189UVPROXY (840682103800), PACS-IW-441, PACS-IW-441TUVSW, PACS-IW-402, PACS-IW-318, MINNETOHE, PACS-IW-253, PACS-IW-581UV, PACS-IW-370, PACS-IW-UVT370, VISOU02345023, VISOU02288781, 1-218291079, 1-103108035, MFHO14767332, PALMDALEM00558700, PALMDALEM01810788, PACS-IW-454, PACS-IW-406, 20101378UBSW, ILCC01373579 (840682103800), ILCC14580319 (840682103800), 516473UVSW (840682103800), JOHNTMA19732280T (840682103800), 1-182669905, NCDC20279342, CENTERFOR01627896, CENTERFOR16023960UVProxy, PACS-IW-176, PACS-IW-176UVTEST, PACS-IW-405, PACS-IW-336, NASONHOSP14898835, RRA01814001, MYRTLEHIL01444483, PSPC01815255, 1-283596904, HOOO20091140, GZMG02182469CNTRLR (840682103800), GZMG02287985 (840682103800), GZMG02288300 (840682103800), PACS-IW-556UV, URSA20025013, PACS-IW-431, 1-598891598, PACS-IW-230, INTERCOAST17594527UVProxy, MDHC16204735UVProxy, 201392UVSW, 505368UVBSW (840682103800), NNAR14767799 (840682103800), PACS-IW-479, PACS-IW-557 (840682103800), URS20583582 (840682103800), PACS-IWUV-481, PACS-IW-476, PACSIW476UVTEST, GGMC02349137, 1-486091448, 1-486091475, 1-750710672, SUC00558667, 1-802428413, 954688UVBSW100, PACS-IW-1511, KDH217192544, ACP00558109, PACS-IW-31Test1, PACS-IW-31Test, ACP01613226, 1-219095008, OKOS14767330, 918277CVUWBSW, CCA20759776SF, PACS-IW-487, QTHBL14767810UVPROXY, QTHBL14767809UVSFBK, QTHBL14767808UVSF1KO, QTHBL14767807UVSFSIM, QTHBL14767806UVSFVAL, QTHBL02256595, VCM02255583T, VCM01819618, VCM02255586TSP, VMC02255587NSP, BOJC00558520, PACS-IW-56, PACS-IW-225, 1-375705893, DDNI14776603, PACS-IW-129, DISSFHW01, 1-644600677, PACS-IW-154UV, FLMC14777071, NEWYORK01291738, OANT02035061, PACS-IW-424CTLR, PACS-IW-424UVN1, PACS-IW-424UVN2, VBHCP20497227, PACS-IW-2635, PREMI02182462, PREMI02182462, NORTHWEST01804127, HCIT4271649UW, AH4325SV01, AH5291PC02, AP6264PC01, AP6469PC01, AH0116SV03, AH0106SV03, HCD4440494UV, HCIT4258559UV, HCIT7109403UV, HCIT4244609UV, HCIT4708563UV, HCIT4470563UV-CTRL, HCIT4261024UVCTRL, HCIT7113573UV, 519264PACSAW1 (840682103800), 416813UV (840682103800), 416813TESTRPACSUV (840682103800), HCIT4266470UW, HCIT4238540UV, HCIT4486723UV, E4167658, X314119802, X141385617, A5485262 / A5485266 / A5485267 / A5485269 / A5485270 / A5485271, A9190177, M41980107, M4487535, M44997011, HC0399UV01, CC4105PC02, PC1695SV01, 786787SV02, HBON01SV02, HC4105PC01, 509940UV01, HC0529PC01, HC0529PC01, 233638UV01, HC0245PC02, 600791PC02, 427990UV01, PC1961SV02, 531344PC01, 434487SV03, PX4900SV02, HC0565PC03, TP0575UV02, GH1077UV01, 083055820116113, 083055824999515, 083055861021012, 83055862088813, 083055800046112, 81111DBS01, IL1469IT05, IL1469IT16, A5992711, A5412010, A6197102, KW0000PP02, HCIT4175024UV, AMS3963, BON0164, ECT0265, HCIT4192962UV, HCIT4264206UW, PL3673RW01, PL1493RW02, PL2970RW01, PL1124RW01, PL1499RW03, PL3349PC01, PL1501RW03, PL2624RW01, PL3249RW02, PL3277RW01, PL1005RW01, 600062UV, PL3362RW01, PL0326RW01, PL2975RW02, PL1504RW02, PL2971RW01, RU9255ID01, RU6968ID01, RU8945ID01, RU7519ID01, RU1781RW01, RU2580ID01, RU4255ID01, RU0003ID01, RU0472ID03, RU9595ID02, RU9327ID02, RU1011ID05, RU8366ID01, RU7808ID02, RU1516ID03, RU1646ID01, RU1112ID02, 01977813, 01980259, RU3052ID01, RU1107RW01, RU1107RW01, RU7175ID01, RU1717ID04, RU9216ID02, RU3453RW03, 600101RW02, RU8002ID01, RU1544ID01, RU1516ID03, RU9940RW01, RU5388ID01, RU0994ID03, RU3794ID01, RU9226ID01, RU9697ID01, 1509505, RU0968ID04, RU0120ID01, RU6164ID01, RU9546ID01, RU7468ID01, RU3998ID01, 600105ID03, SA2402PP02, SA2110PP05, SA1339PP03, ZA2541UV01, ZA2414PAC1, ZA2415PAC1, ZA2474UV01, ZA2267PAC1, ZA1058UV01, ZA2551PAC1, ZA1058UV01, ZA2412PAC2, ZA2472PAC2, ZA000010, ZA2412PAC2, MPX35219, DP760316, FP502804, 802030PC01, 228493WS01, 124774CS01, 482896SV03, 06051PAC04, HCIT4133734PACS, HCIT4148106PEE, Others Tracked under Service Cloud product ID. 2. Model Number: 2088026-723 (Centricity Universal Viewer with PACS-IW foundation software versions 6.0 through 6.0 SP7.1); UDI-DI: 840682103800; System ID: NYHOSPI16204605, NYHOSPI16204606, NYHOSPI16204607, NYHOSPI16204608, NYHOSPI16204609, NYHOSPI16204612, NYHOSPI16204613. 3. Model Number: 2102676-001 (Centricity Universal Viewer with PACS-IW foundation software versions 6.0 through 6.0 SP7.1); UDI-DI: 840682103800; System ID: PACS-IW-119. 4. Model Number: 2104867-044 (Centricity Universal Viewer with PACS-IW foundation software versions 6.0 through 6.0 SP7.1); UDI-DI: 840682103800; System ID: DDOC02339896.

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Z-1511-2022 Class II Service manuals for the CT, PET, or NM table as... Jun 2, 2022

Frequently Asked Questions

Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.

Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.

Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.

What Should You Do?

Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.

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