# FDA recall Z-2265-2024

> **Abbott Medical** · Class II · device recall initiated 2024-05-16.

## Product

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

## 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.

## Key facts

- **Recall number:** Z-2265-2024
- **Recalling firm:** Abbott Medical
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-16
- **Report date:** 2024-07-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Plano, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2265-2024

## Citation

> AI Analytics. FDA recall Z-2265-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2265-2024. Source: US FDA. Licensed CC0.

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