No image published for this recall

Abbotts proclaim™ scs proclaim™ drg infinity™ dbs implantable pulse generators

Official notice

30 Apr 2026

MediumHealth Canada

An official Health Canada notice concerns Abbotts proclaim™ scs proclaim™ drg infinity™ dbs implantable pulse generators. Abbott is sharing important information regarding the Infinity™ Deep Brain Stimulation (DBS) Neurostimulation System, Proclaim™ Spinal Cord Stimulation (SCS) and Proclaim™ Dorsal Root Ganglion (DRG) Neurostimulation Systems. The purpose of this communication is to remind health care providers that the systems contain a Surgery Mode feature designed to help protect the implanted device from potential interference associated with the use of electrosurgical units (ESUs) during certain surgical procedures. Published 2026-04-30.

What to do now

Contact the manufacturer if you require additional information.

Recall number

81998

Official notice

2026-04-30

The hazard

Abbott is sharing important information regarding the Infinity™ Deep Brain Stimulation (DBS) Neurostimulation System, Proclaim™ Spinal Cord Stimulation (SCS) and Proclaim™ Dorsal Root Ganglion (DRG) Neurostimulation Systems. The purpose of this communication is to remind health care providers that the systems contain a Surgery Mode feature designed to help protect the implanted device from potential interference associated with the use of electrosurgical units (ESUs) during certain surgical procedures.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Skus

6660, 6661, 3660, 3662, 3665, 3661, 3667, 3663, 3664, 6663, 6662

Other

RA RA-81998

Model Numbers

6660, 6661, 3660, 3662, 3665, 3661, 3667, 3663, 3664, 6663, 6662

Recall Numbers

81998

Checked manually this time?

The app alerts you when a new official recall is published — no searching, no checking back.

Turn on recall alerts

Affected products

Product 1

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 6660

Product 2

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 6661

Product 3

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 3660

Product 4

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 3662

Product 5

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 3665

Product 6

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 3661

Product 7

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 3667

Product 8

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 3663

Product 9

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 3664

Product 10

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 6663

Product 11

Lot or serial number - More than 100 numbers, contact manufacturer., Model or catalogue number - 6662

Risk / hazard

Abbott is sharing important information regarding the Infinity™ Deep Brain Stimulation (DBS) Neurostimulation System, Proclaim™ Spinal Cord Stimulation (SCS) and Proclaim™ Dorsal Root Ganglion (DRG) Neurostimulation Systems. The purpose of this communication is to remind health care providers that the systems contain a Surgery Mode feature designed to help protect the implanted device from potential interference associated with the use of electrosurgical units (ESUs) during certain surgical procedures.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Abbott Medical.

Source & status

Source

Health Canada

Tier

beta

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

81998

Classification

Type II

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
Something wrong on this page?

Related recalls

HEALTH
Critical

Centrimag™ adult ecmo kit and blood pump

Health Canada22 Oct 2025

Brand match

Critical risk

Markets

CA
HEALTH
High

Heartmate 3™ system controller

Health Canada17 Oct 2025

Brand match

High risk

Markets

CA
HEALTH
Medium

Eterna™ implantable pulse generator

Health Canada15 Oct 2025

Brand match

Medium risk

Markets

CA
HEALTH
Medium

Tactiflex™ ablation catheter, sensor enabled™

Health Canada17 Sept 2025

Brand match

Medium risk

Markets

CA
HEALTH
Medium

Mobile power unit

Health Canada9 Jul 2025

Brand match

Medium risk

Markets

CA
HEALTH
Medium

Amplatzer torqvue delivery system

Health Canada26 Mar 2025

Brand match

Medium risk

Markets

CA
HEALTH
Medium

Cardiomems patient electronics system

Health Canada18 Oct 2024

Brand match

Medium risk

Markets

CA
HEALTH
Medium

Aveir™ leadless pacemaker

Health Canada19 Aug 2024

Brand match

Medium risk

Markets

CA
HEALTH
Medium

Heartmate 3 lvas implant kit and heartmate 3 system controller

Health Canada30 Jul 2024

Brand match

Medium risk

Markets

CA
HEALTH
Medium

Proclaim implantable pulse generators

Health Canada4 Jul 2024

Brand match

Medium risk

Markets

CA
HEALTH
Medium

Infinity 5 and 7 implantable pulse generator

Health Canada3 Jul 2024

Brand match

Medium risk

Markets

CA
HEALTH
Medium

2Nd generation centrimag™ primary console with em-tec adult flow probe

Health Canada14 Jun 2024

Brand match

Medium risk

Markets

CA

Weekly recall digest

Get next week's recalls before you need them.

One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.

The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.

This recall was published 30 Apr 2026. The next one won't wait for you to search.

RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.