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Versapulse dual wavelength and co2 laser systems

Official notice

13 May 2026

Last checked

13 May 2026

Medium riskHealth Canada

An official Health Canada notice concerns Versapulse dual wavelength and co2 laser systems. Boston Scientific has identified that service manuals for the VersaPulse (VPPs) Dual Wavelength (DW) and CO2 laser systems include incorrect or incomplete laser safety eyewear protection information, resulting in the potential for ocular harm. Published 2026-05-13.

What to do now

Contact the manufacturer if you require additional information.

Recall number

82062

Official notice

2026-05-13

The hazard

Boston Scientific has identified that service manuals for the VersaPulse (VPPs) Dual Wavelength (DW) and CO2 laser systems include incorrect or incomplete laser safety eyewear protection information, resulting in the potential for ocular harm.

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.

Lots

Service Manual PN SM-0000400, Service Manual PN 0636-499-00, Service Manual PN PB0000300, Service Manual PN PB0000301

Skus

GA-2000000, 0638-800-01, GA-1000000, GA-0000140

Other

RA RA-82062

Model Numbers

GA-2000000, 0638-800-01, GA-1000000, GA-0000140

Recall Numbers

82062

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Affected products

Product 1

Lot or serial number - Service Manual PN SM-0000400, Model or catalogue number - GA-2000000

Product 2

Lot or serial number - Service Manual PN 0636-499-00, Model or catalogue number - 0638-800-01

Product 3

Lot or serial number - Service Manual PN PB0000300, Model or catalogue number - GA-1000000

Product 4

Lot or serial number - Service Manual PN PB0000301, Model or catalogue number - GA-0000140

Risk / hazard

Boston Scientific has identified that service manuals for the VersaPulse (VPPs) Dual Wavelength (DW) and CO2 laser systems include incorrect or incomplete laser safety eyewear protection information, resulting in the potential for ocular harm.

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: Lumenis.

Source & status

Source

Health Canada

Tier

beta

Category

HOME

Classification

Type II

App estimate

medium

Recall details

Recall number

82062

Classification

Type II

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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