No image published for this recall

Harmonyair a-series surgical lighting system and alyon surgical lighting system

Official notice

21 May 2026

MediumHealth Canada

An official Health Canada notice concerns Harmonyair a-series surgical lighting system and alyon surgical lighting system. Steris identified through customer complaints that on Harmonyair A-Series Lighting System and Alyon Surgical Lighting System the plus/minus (+/-) buttons that control light intensity on the light heads may detach. If detachment occurs during a patient procedure, the buttons could enter the sterile field and disrupt the procedure resulting in a procedure delay. Users can continue to use their lighting system(s) prior to completion of the correction. Users are reminded to ensure no excess fluids remain on light head during or after cleaning, per the operator manual. Should detachment of the plus/minus (+/-) buttons occur prior to the correction being completed, users should immediately contact their local Steris representative. Published 2026-05-21.

What to do now

Contact the manufacturer if you require additional information.

Recall number

82097

Official notice

2026-05-21

The hazard

Steris identified through customer complaints that on Harmonyair A-Series Lighting System and Alyon Surgical Lighting System the plus/minus (+/-) buttons that control light intensity on the light heads may detach. If detachment occurs during a patient procedure, the buttons could enter the sterile field and disrupt the procedure resulting in a procedure delay. Users can continue to use their lighting system(s) prior to completion of the correction. Users are reminded to ensure no excess fluids remain on light head during or after cleaning, per the operator manual. Should detachment of the plus/minus (+/-) buttons occur prior to the correction being completed, users should immediately contact their local Steris representative.

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

0000002L, 00003A2V, 00003A2L, 003A2A1L, 00003A2LT, 00003L2V, 004A3L2V, 004A3L2VT, 00003L2L, 004A3L2L, 1955038X, 13A11L09F, 00013A11F, 11041370, 00000011L, 00011L09F, 00011L09L, 13V11L09L

Other

RA RA-82097

Model Numbers

0000002L, 00003A2V, 00003A2L, 003A2A1L, 00003A2LT, 00003L2V, 004A3L2V, 004A3L2VT, 00003L2L, 004A3L2L, 1955038X, 13A11L09F, 00013A11F, 11041370, 00000011L, 00011L09F, 00011L09L, 13V11L09L

Recall Numbers

82097

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 10 numbers, contact manufacturer., Model or catalogue number - 0000002L

Product 2

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 00003A2V

Product 3

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 00003A2L

Product 4

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 003A2A1L

Product 5

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 00003A2LT

Product 6

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 00003L2V

Product 7

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 004A3L2V

Product 8

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 004A3L2VT

Product 9

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 00003L2L

Product 10

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 004A3L2L

Product 11

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 1955038X

Product 12

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 13A11L09F

Product 13

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 00013A11F

Product 14

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 11041370

Product 15

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 00000011L

Product 16

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 00011L09F

Product 17

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 00011L09L

Product 18

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 13V11L09L

Risk / hazard

Steris identified through customer complaints that on Harmonyair A-Series Lighting System and Alyon Surgical Lighting System the plus/minus (+/-) buttons that control light intensity on the light heads may detach. If detachment occurs during a patient procedure, the buttons could enter the sterile field and disrupt the procedure resulting in a procedure delay. Users can continue to use their lighting system(s) prior to completion of the correction. Users are reminded to ensure no excess fluids remain on light head during or after cleaning, per the operator manual. Should detachment of the plus/minus (+/-) buttons occur prior to the correction being completed, users should immediately contact their local Steris representative.

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

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Steris.

Source & status

Source

Health Canada

Tier

beta

Category

HOME

Classification

Type II

App estimate

medium

Recall details

Recall number

82097

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

HOME
Medium

Harmonyair a-series surgical lighting system

Health Canada12 May 2026

Brand match

Medium risk

Markets

CA
HOME
Medium

Dual flat panel monitor (dfpm) accessory to the harmonyair® a-series and e-series surgical lighting systems

Health Canada24 Jun 2025

Brand match

Medium risk

Markets

CA
HOME
Medium

Sterile light handle cover

Health Canada24 Mar 2023

Brand match

Medium risk

Markets

CA
ELECTRONICS
Medium

a product listed in the official notice - safety alert

FDA14 Oct 2026

Brand match

Medium risk

Markets

CA
HOME
Critical

Solar™ gi

Health Canada16 Jul 2026

Brand match

Critical risk

Markets

CA
HOME
Medium

Omni-tract surgical retractor system

Health Canada3 Jul 2026

Brand match

Medium risk

Markets

CA
HOME
Medium

Urinary catheter trays containing cliniclean pericare wipes

Health Canada3 Jul 2026

Brand match

Medium risk

Markets

CA
HOME
Medium

Wasplab

Health Canada2 Jul 2026

Brand match

Medium risk

Markets

CA
HOME
Medium

Nephromax high pressure nephrostomy balloon catheter

Health Canada2 Jul 2026

Brand match

Medium risk

Markets

CA
HOME
Medium

Uhi-4 high flow insufflation system - insufflator

Health Canada24 Jun 2026

Brand match

Medium risk

Markets

CA
HOME
Medium

Atellica ch enzymatic hemoglobin a1c (a1c e) assay

Health Canada18 Jun 2026

Brand match

Medium risk

Markets

CA
HOME
Medium

Iceman classic3™

Health Canada3 Jun 2026

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 21 May 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.