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No image published for this recall

Smartmix tips combi

Official notice

26 Feb 2026

Last checked

26 Feb 2026

Medium riskHealth Canada

An official Health Canada notice concerns Smartmix tips combi. The recall must be done due to misclassification which led to the sale of unlicensed medical devices. Therefore, no real or potential defectiveness is suspected. Nevertheless, users should stop using the refill tips. Published 2026-02-26.

What to do now

Contact the manufacturer if you require additional information.

Recall number

81646

Official notice

2026-02-26

The hazard

The recall must be done due to misclassification which led to the sale of unlicensed medical devices. Therefore, no real or potential defectiveness is suspected. Nevertheless, users should stop using the refill tips.

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

316509, 296180, 283063, 254452, 266638, 305728, 273737, 292229, 283601, 270232, 303632, 290199, 316511, 279178, 250354, 294552, 316512, 322758, 287187, 294551, 240985, 290207

Skus

212042, 110991, 211759, 110424, 110728

Other

RA RA-81646

Model Numbers

212042, 110991, 211759, 110424, 110728

Recall Numbers

81646

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Affected products

Product 1

Lot or serial number - 316509, Model or catalogue number - 212042

Product 2

Lot or serial number - 296180, Model or catalogue number - 212042

Product 3

Lot or serial number - 283063, Model or catalogue number - 212042

Product 4

Lot or serial number - 254452, Model or catalogue number - 212042

Product 5

Lot or serial number - 266638, Model or catalogue number - 212042

Product 6

Lot or serial number - 305728, Model or catalogue number - 212042

Product 7

Lot or serial number - 273737, Model or catalogue number - 110991

Product 8

Lot or serial number - 292229, Model or catalogue number - 110991

Product 9

Lot or serial number - 283601, Model or catalogue number - 211759

Product 10

Lot or serial number - 270232, Model or catalogue number - 211759

Product 11

Lot or serial number - 303632, Model or catalogue number - 211759

Product 12

Lot or serial number - 290199, Model or catalogue number - 211759

Product 13

Lot or serial number - 316511, Model or catalogue number - 211759

Product 14

Lot or serial number - 279178, Model or catalogue number - 211759

Product 15

Lot or serial number - 250354, Model or catalogue number - 211759

Product 16

Lot or serial number - 294552, Model or catalogue number - 211759

Product 17

Lot or serial number - 316512, Model or catalogue number - 110424

Product 18

Lot or serial number - 322758, Model or catalogue number - 110424

Product 19

Lot or serial number - 287187, Model or catalogue number - 110728

Product 20

Lot or serial number - 294551, Model or catalogue number - 110728

Product 21

Lot or serial number - 240985, Model or catalogue number - 110728

Product 22

Lot or serial number - 290207, Model or catalogue number - 110728

Risk / hazard

The recall must be done due to misclassification which led to the sale of unlicensed medical devices. Therefore, no real or potential defectiveness is suspected. Nevertheless, users should stop using the refill tips.

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: Dmg Chemisch-pharmazeutische Fabrik.

Source & status

Source

Health Canada

Tier

beta

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

81646

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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