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Brevera® breast biopsy system

Official notice

14 Jan 2026

Last checked

14 Jan 2026

Medium riskHealth Canada
Watch Hologic

An official Health Canada notice concerns Brevera® breast biopsy system. The subject device is being removed because there is a risk of metal and plastic particles being dislodged from the device during use. Published 2026-01-14.

What to do now

Quarantine any subject product units you currently have in your inventory and return the subject product to Hologic. Do not use the subject product.

Recall number

81482

Official notice

2026-01-14

The hazard

The subject device is being removed because there is a risk of metal and plastic particles being dislodged from the device during use.

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

BREVDISP09

Other

RA RA-81482

Model Numbers

BREVDISP09

Recall Numbers

81482

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Affected products

Product 1

Affected products - Brevera® Breast Biopsy System, Affected products - Not applicable., Model or catalogue number - BREVDISP09

Product 2

Model or catalogue number - BREVDISP09

Risk / hazard

The subject device is being removed because there is a risk of metal and plastic particles being dislodged from the device during use.

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

Hologic

Manufacturer

Not provided

Phone

Not provided

Brand: Hologic.

Source & status

Source

Health Canada

Tier

official

Category

HOME

Classification

Type II

App estimate

medium

Recall details

Recall number

81482

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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