Recall image placeholder

No image published for this recall

Leksell gamma knives

Official notice

18 Feb 2026

Last checked

18 Feb 2026

Medium riskHealth Canada
Watch Elekta

An official Health Canada notice concerns Leksell gamma knives. When treating patients with the Leksell Gamma Knife®, the patient is attached to the device via an adapter. The adapter is the interface between the Leksell Gamma Knife® and the immobilization system used for the treatment. The Leksell Gamma Knife® has three types of adapters for patient fixation, the g-frame adapter, the vantage adapter, and the mask adapter. Elekta has become aware that a Quality Assurance (QA) procedure was initiated while the adapter was not properly locked to the patient positioning system of the Leksell Gamma Knife® as a result, the QA check failed. Published 2026-02-18.

What to do now

Elekta will issue a Field Safety Notice on 18 Feb 2026 for affected Gamme Knife and Elekta Esprit devices. The IFU will be updated to include a new warning.

Recall number

81619

Official notice

2026-02-18

The hazard

When treating patients with the Leksell Gamma Knife®, the patient is attached to the device via an adapter. The adapter is the interface between the Leksell Gamma Knife® and the immobilization system used for the treatment. The Leksell Gamma Knife® has three types of adapters for patient fixation, the g-frame adapter, the vantage adapter, and the mask adapter. Elekta has become aware that a Quality Assurance (QA) procedure was initiated while the adapter was not properly locked to the patient positioning system of the Leksell Gamma Knife® as a result, the QA check failed.

How to check if you're affected

Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.

Skus

715000, 1016200, 1110200

Other

RA RA-81619

Model Numbers

715000, 1016200, 1110200

Recall Numbers

81619

Checked manually this time?

The app watches your VIN and alerts you automatically next time — no searching, no checking back.

Turn on automatic VIN checks

Affected products

Product 1

Lot or serial number - All lots., Model or catalogue number - 715000

Product 2

Lot or serial number - All lots., Model or catalogue number - 1016200

Product 3

Lot or serial number - All lots., Model or catalogue number - 1110200

Risk / hazard

When treating patients with the Leksell Gamma Knife®, the patient is attached to the device via an adapter. The adapter is the interface between the Leksell Gamma Knife® and the immobilization system used for the treatment. The Leksell Gamma Knife® has three types of adapters for patient fixation, the g-frame adapter, the vantage adapter, and the mask adapter. Elekta has become aware that a Quality Assurance (QA) procedure was initiated while the adapter was not properly locked to the patient positioning system of the Leksell Gamma Knife® as a result, the QA check failed.

Where it was sold

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

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Brand

Elekta

Manufacturer

Not provided

Phone

Not provided

Brand: Elekta.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

81619

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
Something wrong on this page?

Related recalls

CA
Recall image placeholder

Mosaiq

Medium riskHealth Canada6 May 2026
CA
Recall image placeholder

Leksell gammaplan®

Critical riskHealth Canada23 Dec 2025
CA
Recall image placeholder

Elekta modulator discharge rod

Critical riskHealth Canada19 Nov 2025
CA
Recall image placeholder

Mosaiq

Medium riskHealth Canada4 Sept 2025
CA
Recall image placeholder

Mosaiq

Medium riskHealth Canada29 Jan 2025
CA
Recall image placeholder

Elekta infinity, elekta synergy and versa hd

Medium riskHealth Canada7 Nov 2023
CA
Recall image placeholder

Aisys, avance, and aespire anesthesia machines

Medium riskHealth Canada2 Jul 2026
CA
Recall image placeholder

Abiomed introducer kits with impella heart pumps

High riskHealth Canada29 Jun 2026
CA
Recall image placeholder

Importation of chinese-authorized ifosfamide for injection due to the current shortage of canadian-authorized ifex (ifosfamide for injection)

Medium riskHealth Canada22 Jun 2026
CA
Recall image placeholder

Cyberknife® treatment delivery system

Medium riskHealth Canada22 Jun 2026
CA
Recall image placeholder

Faradrive™ steerable sheath

Medium riskHealth Canada19 Jun 2026
CA
Recall image placeholder

Ge healthcare integrated and stand-alone resuscitation systems

Medium riskHealth Canada16 Jun 2026

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 18 Feb 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.