Boston Scientific CRM Corp VITALITY AVT (model A155). Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies. Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
VITALITY AVT (model A155). Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies. Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA.
Brand
Boston Scientific CRM Corp
Lot Codes / Batch Numbers
Model A155, serial numbers: 112541, 112542, 112543, 112544, 112551, 112552, 112553, 112555, 112566, 112602, 112611, 112616, 112619, 112620, 112621, 112623, 112626, 112627, 112628, 112631, 112632, 112633, 112635, 112636, 112640, 112641, 112643, 112645, 112646, 112647, 112648, 112650, 112651, 112652, 112654, 112655, 112656, 112657, 112658, 112661, 112662, 112663, 112664, 112665, 112666, 112672, 112673, 112675, 112679, 112680, 112681, 112682, 112684, 112685, 112686, 112687, 112688, 112691, 112694, 112695, 112696, 112697, 112698, 112699, 112701, 112702, 112703, 112704, 112706, 112708, 112709, 112710, 112713, 112714, 112715, 112716, 112718, 112719, 112721, 112722, 112725, 112729, 112730, 112733, 112735, 112738, 112739, 112740, 112773, 112777, 112778, 112846, 112849, 112850, 112851, 112852, 112853, 112854, 112855, 112856, 112859, 112860, 112861, 112863, 112865, 112892, 113009, 113011, 113078, 113079, 113167, 113184, 113185, 113189, 113196, 113200, 113201, 113202, 113205, 113207, 113209, 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115267, 115268, 115269, 115270, 115271, 115272, 115274, 115275, 115276, 115277, 115283, 115289, 115290, 115305, 115306, 115310, 115313, 115344, 115347, 115348, 115352, 115370, 115375, 115402, 115410, 115416, 115472, 115488, 115497, 115529, 115539, 115555, 115562, 115616, 115619, 115628, 115639, 115652, 115667, 115671, 115674, 115678, 115679, 115680, 115682, 115686, 115687, 115700, 115703, 115712, 115732, 115733, 115739, 115743, 115754, 115760, 115782, 115795, 115799, 115830, 115859, 115875, 115879, 115977, 116030, 116067, 116069, 116083, 116084, 116087, 116097, 116101.
Products Sold
Model A155, serial numbers: 112541, 112542, 112543, 112544, 112551, 112552, 112553, 112555, 112566, 112602, 112611, 112616, 112619, 112620, 112621, 112623, 112626, 112627, 112628, 112631, 112632, 112633, 112635, 112636, 112640, 112641, 112643, 112645, 112646, 112647, 112648, 112650, 112651, 112652, 112654, 112655, 112656, 112657, 112658, 112661, 112662, 112663, 112664, 112665, 112666, 112672, 112673, 112675, 112679, 112680, 112681, 112682, 112684, 112685, 112686, 112687, 112688, 112691, 112694, 112695, 112696, 112697, 112698, 112699, 112701, 112702, 112703, 112704, 112706, 112708, 112709, 112710, 112713, 112714, 112715, 112716, 112718, 112719, 112721, 112722, 112725, 112729, 112730, 112733, 112735, 112738, 112739, 112740, 112773, 112777, 112778, 112846, 112849, 112850, 112851, 112852, 112853, 112854, 112855, 112856, 112859, 112860, 112861, 112863, 112865, 112892, 113009, 113011, 113078, 113079, 113167, 113184, 113185, 113189, 113196, 113200, 113201, 113202, 113205, 113207, 113209, 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Boston Scientific CRM Corp is recalling VITALITY AVT (model A155). Implantable Cardioverter Defibrillator. Atrial and Ventricular Therapies. due to Boston Scientific has recently identified low-voltage capacitors from a former supplier that may be subject to degradation at a low rate of occurrence. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Boston Scientific has recently identified low-voltage capacitors from a former supplier that may be subject to degradation at a low rate of occurrence. These capacitors may cause accelerated battery depletion and may reduce the time between elective replacement indicator (ERI) and end of life (EOL) to less than 3 months.
Recommended Action
Per FDA guidance
An Urgent Medical Devivce Information letter dated April 05, 2007 was sent to implanting and following physicians. The letter describes the issue, identifies patients with affected devices and provides recommendations.
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