Abbott Laboratories Inc. (St Jude Medical) NeuroTherm NT2000iX Radiofrequency (RF) Generator, Model Number RFG-NT-2000 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
NeuroTherm NT2000iX Radiofrequency (RF) Generator, Model Number RFG-NT-2000
Brand
Abbott Laboratories Inc. (St Jude Medical)
Lot Codes / Batch Numbers
UDI 05415067022417: Serial Numbers: 18675078, 18709738, 18097502, 18023105, 18739462, 18650501, 18493702, 18718469, 18666645, 18634334, 18666647, 18427317, 18742999, 18709732, 18222185, 18222187, 18240730, 18201200, 18743003, 18343825, 18088294, 18201198, 18222190, 18240731, 17991994, 18132016, 18500164, 18522935, 18659497, 18750318, 18854584, 18718473, 18873320, 18240735, 18102325, 18648497, 18666643, 18666646, 18657521, 17991999, 18313159, 18614034, 18721060, 18493705, 18493709, 18610701, 18302046, 18192751, 18132012, 18222188, 18240728, 18718472, 18500167, 18132008, 18493711, 18313153, 17905956, 18060073, 18132011, 18102323, 18014268, 18014258, 18343824, 18240733, 18180086, 18675069, 18060017, 18060067, 18060071, 17964784, 18427318, 18648518, 18675068, 18648648, 18192752, 18709733, 18709734, 18302042, 18265068, 18659496, 18192753, 18192756, 18222183, 18522719, 18705743, 18522937, 18644839, 18873319, 18102324, 18088297, 18659489, 18706571, 18192754, 18622842, 18240729, 18180085, 18659495, 18187525, 18192750, 18115250, 18714394, 18666648, 18070518, 18072514, 18180082, 18634336, 18699641, 18854582, 18522709, 18704516, 18493701, 18716594, 18709741, 18873321, 18302048, 18644838, 18699645, 18102337, 18555754, 18743000, 18690921, 18180088, 18657520, 18522715, 18343821, 18201195, 18648650, 18522714, 18265071, 18709739, 18709735, 18023104, 18313165, 18070527, 18648652, 18650503, 18265072, 18666650, 18634337, 18313157, 18533473, 18648647, 18705742, 18644824, 18493707, 18699643, 18265070, 18343819, 17905963, 18070525, 18750319, 18343820, 18343823, 18650500, 17991997, 18701492, 18742994, 18014262, 18709742, 18854581, 18427321, 18659494, 18659493, 18644840, 18500166, 18533504, 18180083, 18427319, 18648008, 18648578, 18690926, 18657519, 18014259, 18014254, 18132092, 18302043, 18132014, 18003308, 18003311, 18003313, 18014255, 18014269, 18659490, 18047384, 18088295, 18014267, 18038591, 18023107, 18003310, 18014261, 18648619, 18648653, 18648655, 18102335, 18265069, 18854583, 18222191, 18014270, 18014271, 18690920, 18302047, 18696583, 18522716, 18427320, 18265066, 18302041, 18699642, 18192749, 18192755, 18675070, 18675076, 17860513, 17942355, 17959675, 17959676, 17959677, 17981234, 17981235, 18003314, 18003325, 18014272, 17860514, 17860515, 17905959, 17905962, 18187528, 18892887, 17905965, 17863602, 18302049, 18500165, 17856739, 18115251, 17856738, 17903459, 18115245, 18115246, 18126612, 18126613, 18500161, 17865145, 17856737, 18187529, 17981236, 17981233, 18132007, 18699646, 18180087, 18699640
Products Sold
UDI 05415067022417: Serial Numbers: 18675078, 18709738, 18097502, 18023105, 18739462, 18650501, 18493702, 18718469, 18666645, 18634334, 18666647, 18427317, 18742999, 18709732, 18222185, 18222187, 18240730, 18201200, 18743003, 18343825, 18088294, 18201198, 18222190, 18240731, 17991994, 18132016, 18500164, 18522935, 18659497, 18750318, 18854584, 18718473, 18873320, 18240735, 18102325, 18648497, 18666643, 18666646, 18657521, 17991999, 18313159, 18614034, 18721060, 18493705, 18493709, 18610701, 18302046, 18192751, 18132012, 18222188, 18240728, 18718472, 18500167, 18132008, 18493711, 18313153, 17905956, 18060073, 18132011, 18102323, 18014268, 18014258, 18343824, 18240733, 18180086, 18675069, 18060017, 18060067, 18060071, 17964784, 18427318, 18648518, 18675068, 18648648, 18192752, 18709733, 18709734, 18302042, 18265068, 18659496, 18192753, 18192756, 18222183, 18522719, 18705743, 18522937, 18644839, 18873319, 18102324, 18088297, 18659489, 18706571, 18192754, 18622842, 18240729, 18180085, 18659495, 18187525, 18192750, 18115250, 18714394, 18666648, 18070518, 18072514, 18180082, 18634336, 18699641, 18854582, 18522709, 18704516, 18493701, 18716594, 18709741, 18873321, 18302048, 18644838, 18699645, 18102337, 18555754, 18743000, 18690921, 18180088, 18657520, 18522715, 18343821, 18201195, 18648650, 18522714, 18265071, 18709739, 18709735, 18023104, 18313165, 18070527, 18648652, 18650503, 18265072, 18666650, 18634337, 18313157, 18533473, 18648647, 18705742, 18644824, 18493707, 18699643, 18265070, 18343819, 17905963, 18070525, 18750319, 18343820, 18343823, 18650500, 17991997, 18701492, 18742994, 18014262, 18709742, 18854581, 18427321, 18659494, 18659493, 18644840, 18500166, 18533504, 18180083, 18427319, 18648008, 18648578, 18690926, 18657519, 18014259, 18014254, 18132092, 18302043, 18132014, 18003308, 18003311, 18003313, 18014255, 18014269, 18659490, 18047384, 18088295, 18014267, 18038591, 18023107, 18003310, 18014261, 18648619, 18648653, 18648655, 18102335, 18265069, 18854583, 18222191, 18014270, 18014271, 18690920, 18302047, 18696583, 18522716, 18427320, 18265066, 18302041, 18699642, 18192749, 18192755, 18675070, 18675076, 17860513, 17942355, 17959675, 17959676, 17959677, 17981234, 17981235, 18003314, 18003325, 18014272, 17860514, 17860515, 17905959, 17905962, 18187528, 18892887, 17905965, 17863602, 18302049, 18500165, 17856739, 18115251, 17856738, 17903459, 18115245, 18115246, 18126612, 18126613, 18500161, 17865145, 17856737, 18187529, 17981236, 17981233, 18132007, 18699646, 18180087, 18699640
Abbott Laboratories Inc. (St Jude Medical) is recalling NeuroTherm NT2000iX Radiofrequency (RF) Generator, Model Number RFG-NT-2000 due to Potential capacitor failure which typically manifests as in inability to provide output on one or more channels. In some instances, users reported a . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential capacitor failure which typically manifests as in inability to provide output on one or more channels. In some instances, users reported a charring/smoky odor or emission.
Recommended Action
Per FDA guidance
The firm issued a medical device correction/service notice beginning on 04/22/2021. The notice discusses device failure and how to identify it. Should the failure present, then firm is requesting return of the device for servicing.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026