The LifeVest® wearable cardioverter-defibrillator (WCD) prevents sudden cardiac death in at-risk patients who are not candidates for an implantable defibrillator. The WCD's safety and efficacy may be impacted by inappropriate shocks (IAS). Assess causes and clinical consequences of WCD inappropriate shocks in survivors of IAS events. The FDA Manufacturers and User Facility Device Experience (MAUDE) database was searched for IAS adverse events (AE) that were reported during 2021 and 2022. A total of 2,568 IAS-AE were found (average # IAS/event: 1.5±1.9; range: 1-48). IAS were caused by tachycardias (1,255, 48.9%), motion artifacts (840, 32.7%), and oversensing (OS) of low-level electrical signals (473, 18.4%) (p<0.001). Tachycardias included atrial fibrillation (AF; 828,32.2%), supraventricular tachycardia (SVT; 333,13.0%), and non-sustained ventricular tachycardia/fibrillation (NSVT/VF; 87, 3.4%). Activities responsible for motion-induced IAS included riding a motorcycle, lawnmower, or tractor (n=128). IAS induced sustained VT or VF in 19 patients that were subsequently terminated by appropriate WCD shocks.Thirty patients fell and suffered physical injuries. Conscious patients (n=1905) did not use the response buttons to abort shocks (47.9%) or used them improperly (20.2%). IAS resulted in 1,190 emergency room visits or hospitalizations, and 17.3% (421/2440) of patients discontinued the WCD after experiencing IAS, especially multiple IAS. The LifeVest WCD may deliver IAS caused by AF, SVT, NSVT/VF, motion artifacts and oversensing of electrical signals. These shocks may be arrhythmogenic, result in injuries, precipitate WCD discontinuation, and they consume medical resources. Improved WCD sensing, rhythm discrimination, and methods to abort IAS are needed.