FDA Device recall Z-2265-2024
Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY
- FDA Device
- Class II
- ongoing
- Published 2024-07-10
On 2024-07-10 the FDA classified a Class II recall of Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY by Abbott Medical, citing 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 da….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2265-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-16 |
| Published | 2024-07-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Abbott Medical |
| Distribution | US |
Product
Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY
Reason
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.
Identifiers
| code_info | UDI-DI: 05415067047663/ Serial Numbers: 20196493 20196495 20196496 20196497 20196498 20196500 20196502 20196503 2019650…UDI-DI: 05415067047663/ Serial Numbers: 20196493 20196495 20196496 20196497 20196498 20196500 20196502 20196503 20196504 20196505 20196506 20196507 20196508 20196509 20196511 20196512 20196513 20196514 20196515 20196516 20196517 20207397 20207398 20207399 20207400 20207401 20207402 20207403 20207404 20207406 20207407 20207408 20207409 20207410 20207411 20207412 20207413 20207416 20207417 20207419 20207420 20207421 20207422 20207423 20207424 20207425 20207427 20207428 20207429 20207430 20207431 20207432 20207433 20207434 20207435 20207436 20207437 20207438 20207441 20207442 20207443 20207445 20207447 20207448 20207449 20207450 20207451 20207452 20207454 20207455 20207456 20207457 20207458 20207459 20207460 20207461 20207462 20207463 20207465 20207466 20207468 20207469 20207470 20207471 20207473 20207474 20207477 20207478 20207481 20207482 20207483 20207484 20207485 20207486 20207487 20207488 20207489 20207490 20207491 20207494 20207495 20208681 20208682 20208683 20208685 20208687 202086 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2265-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.