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Class IIOngoingZ-0458-2026

Abbott Medical recalls Eterna SCS IPG (Implantable Pulse Generator)

Abbott MedicalPlano, TX, United StatesReported Nov 19, 2025 · 8 months ago
Legal News Analyst ·

Reason for recall

There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS) Implantable Pulse Generators (IPGs), Model 62400 . These devicess may experience a loss of communication with the Clinician Programmer (CP) and/or the Patient Controller (PC).

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • Eterna SCS IPG (Implantable Pulse Generator), Model Number32400
    400 affected lots
    1940001519400017194000201940002119400022194000231940002519400026
    +392 more1940002919400030194000311940003319400035194000371940003819400039194000401940004119400042194000431940004419400045194000481940005119473833194738341947383519473836194738371947383819473839194738401947384119473842194738431947384519473850194738511947385219473853194738541947385519473857194738591947386119473862194738661947386719473870194757561947575919475762194757631947576519475767194757681947577019475771194757721947577419475776194757771947577819475779194757801947578119475782194757831947578419475785194757881947578919475791194757931947579419475796194757991947580019475802194758041947580519475807194758091947581019475811194758121947581319475815194758161947581819475823194758241947582519475826194758271947582919475830194758321947583319475834194758351949339519493397194933981949339919493401194934021949340319493404194934051949340619493407194934081949341019493411194934151949341619493417194934181949342119493422194934231949342419493425194934261949342719493428194934291949343119493432194934331949343419493435194934361949343719493438194934391949344019493442194934451949344619493447194934481949344919493450194934511949345319493454194934551949345619493458194934591949346019493461194934621949346319493465194934661949346719493468194934691949347019493471194934721949347319493474194934771949347819493479194934811949348219493484194934851949348619493488194934891949349019493491194934921949349319524296195242971952429819524299195243001952430319524304195243051952430619524307195243081952430919524310195243111952431219524313195243141952431519524317195243181952431919524320195243211952432219524323195243241952432519524326195243271952432819524329195243301952433119524332195243331952433419524335195243361952433719524338195243391952434019524341195243421952434319524344195243451952434619524347195243481952434919524351195243521952435319524355195243561952435719524358195243601952436119524363195243641952436519524366195243671952436819524369195243701952437219524373195243741952437519524376195243771952437819524379195243801952438119524382195243831952438419524385195243861952438819524389195243901952439119524392195243931952439419524395195114881951150019511540195115541951145619511457195114591951146019511462195114631951146419511465195114661951146719511468195114711951147219511473195114741951147519511477195114781951148019511481195114821951148319511484195114851951148619511487195114891951149019511491195114921951149319511494195114961951149719511498195114991951150119511502195115031951150419511506195115071951150819511510195115111951151219511513195115141951151519511516195115171951151919511520195115211951152219511523195115241951152519511526195115271951152919511530195115311951153219511533195115341951153519511536195115371951153819511539195115411951154219511543195115441951154519511546195115471951154819511549195115501951155219511555195138641951386519513867195138681951386919513870195138731951387419513875195138761951387719513878195138791951388019513881195138821951388319513884195138851951388619513887195138881951388919513890195138911951389219513893195138941951389519513896195138971951389819513899195139001951390219513903195139041951390519513906195139071951390819513909

What the firm is doing

On 10/01/2025 Abbott issued an URGENT MEDCIAL DEVICE RECALL NOTICE to its consignees via email and mail. The notice explained the issue and requested the devices not be implanted, and informed the consignee that a representative would remove the affected devices. Abbott issued an URGENT MEDICAL DEVICE CORRECTION notice to its consignees on 10/06/2025 via email and mail using a traceable means. The notice explained the issued and provided the following patient management guidance: "There are various factors that can lead to BLE communication loss between an IPG and CP/PC, and not all instances are related to this identified component issue. If the PC and/or CP is unable to communicate with the patient's IPG, the troubleshooting steps outlined below, as well as those provided in the Troubleshooting section of CP (Model 55600) and PC (Models 55500, 3876) Instructions for Use may help restore communication. " Use the CP to confirm communication with the IPG during the implant procedure and verify that BLE connectivity is functioning. In some cases, this issue may be detected prior to implantation. " Ensure that Bluetooth wireless connectivity is enabled on both the CP and PC. " Reduce the distance between the CP/PC and the IPG and confirm there are no physical obstructions. Maintaining a clear line of sight may improve communication. " Move away from potential sources of wireless interference, such as household appliances, Wi-Fi routers, electrical equipment, or other wireless devices. " Do not operate other wireless devices at the same time and disconnect any Bluetooth wireless technology media accessories. " If the problem persists, contact your Abbott representative or Abbott Technical Support (1-800-727-7846) for help to determine whether the inability to communicate is related to this issue." Actions to be Taken: Please return a completed Acknowledgement Form and maintain a record of this notice along with a copy of the completed Acknowledgement Form.

DistributionShow details

Worldwide distribution.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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