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Medline convenience kits containing select polycarbonate colored syringes

Official notice

30 Apr 2026

MediumHealth Canada

An official Health Canada notice concerns Medline convenience kits containing select polycarbonate colored syringes. Specific item(s) and lot(s) of Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes are recalled, after identifying unapproved design changes to the products outside of the 510(k) cleared by FDA. Customers must discard the affected products, but all remaining products inside of the kit may be used. Published 2026-04-30.

What to do now

Contact the manufacturer if you require additional information.

Recall number

82000

Official notice

2026-04-30

The hazard

Specific item(s) and lot(s) of Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes are recalled, after identifying unapproved design changes to the products outside of the 510(k) cleared by FDA. Customers must discard the affected products, but all remaining products inside of the kit may be used.

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

24ABS765, 24ABR871, 24ABT556, 21FBM893

Skus

DYNJ41941D, DYNJ53744B, DYNJ56311A, DYNJ41792G, DYNJ49593A

Other

RA RA-82000

Model Numbers

DYNJ41941D, DYNJ53744B, DYNJ56311A, DYNJ41792G, DYNJ49593A

Recall Numbers

82000

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Affected products

Product 1

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - DYNJ41941D

Product 2

Lot or serial number - 24ABS765, Model or catalogue number - DYNJ53744B

Product 3

Lot or serial number - 24ABR871, Model or catalogue number - DYNJ56311A

Product 4

Lot or serial number - 24ABT556, Model or catalogue number - DYNJ41792G

Product 5

Lot or serial number - 21FBM893, Model or catalogue number - DYNJ49593A

Risk / hazard

Specific item(s) and lot(s) of Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes are recalled, after identifying unapproved design changes to the products outside of the 510(k) cleared by FDA. Customers must discard the affected products, but all remaining products inside of the kit may be used.

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: Medline Lp.

Source & status

Source

Health Canada

Tier

beta

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

82000

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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