Class II

Medical Device Recall: Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY

Abbott Medical · May 16, 2024

Reason for Recall

Deep brain stimulation system will first turn off after approximately 50 days after the system is activated and subsequently, this same action will recur approximately every 50 days thereafter. This unexpected lost of stimulation may result in loss of therapy.

Distribution

US: Nationwide distribution including in the states of AZ, CA, CO, DC, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NE, NH, NJ, NY, OH OK, OR, PA, SC, SD, TX, UT, WI, WV.

States Affected

NATIONWIDE

Quantity Affected

302 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2265-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.