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Abbott Medical recalls Abbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO
Recalled May 8, 2024 · FDA recall Z-1695-2024 · Abbott Medical
Hazard
Their is a potential that electromagnetic interference may cause leadless pacemaker may result in mode change. · FDA Class II
Units
10,610 units
Sold at
US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV. OUS: Pending
Description
Their is a potential that electromagnetic interference may cause leadless pacemaker may result in mode change.
Product
Abbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO
Manufacturer(s)
Abbott Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →