No image published for this recall

No image published for this recall

Hickman™ and broviac™ central venous catheter kits

Official notice

20 Jan 2026

Last checked

20 Jan 2026

Medium riskHealth Canada

An official Health Canada notice concerns Hickman™ and broviac™ central venous catheter kits. BD has identified via internal inspections that the packaging of some Hickman catheter and Broviac catheter kits may have damage present on the outer tray, potentially compromising the sterile barrier. This product features a double-tray packaging structure (outer tray and inner tray). The inner tray, which contains the catheter and accessories, is sealed inside the outer tray along with the instructions for use. The sterility of the outer surface of the inner tray and the instructions for use may be compromised. Published 2026-01-20.

What to do now

Contact the manufacturer if you require additional information.

Recall number

81509

Official notice

2026-01-20

The hazard

BD has identified via internal inspections that the packaging of some Hickman catheter and Broviac catheter kits may have damage present on the outer tray, potentially compromising the sterile barrier. This product features a double-tray packaging structure (outer tray and inner tray). The inner tray, which contains the catheter and accessories, is sealed inside the outer tray along with the instructions for use. The sterility of the outer surface of the inner tray and the instructions for use may be compromised.

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

HUKR0065, HUKU0279, HUKU0270, HUKQ0535, HUKU0311, HUKS0776

Skus

0600350, 0600570, 0600620, 0600540, 0600650, 0600560

Other

RA RA-81509

Model Numbers

0600350, 0600570, 0600620, 0600540, 0600650, 0600560

Recall Numbers

81509

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Affected products

Product 1

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 0600350

Product 2

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 0600570

Product 3

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 0600620

Product 4

Lot or serial number - HUKR0065, Model or catalogue number - 0600540

Product 5

Lot or serial number - HUKU0279, Model or catalogue number - 0600540

Product 6

Lot or serial number - HUKU0270, Model or catalogue number - 0600540

Product 7

Lot or serial number - HUKQ0535, Model or catalogue number - 0600650

Product 8

Lot or serial number - HUKU0311, Model or catalogue number - 0600560

Product 9

Lot or serial number - HUKS0776, Model or catalogue number - 0600560

Risk / hazard

BD has identified via internal inspections that the packaging of some Hickman catheter and Broviac catheter kits may have damage present on the outer tray, potentially compromising the sterile barrier. This product features a double-tray packaging structure (outer tray and inner tray). The inner tray, which contains the catheter and accessories, is sealed inside the outer tray along with the instructions for use. The sterility of the outer surface of the inner tray and the instructions for use may be compromised.

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: Bard Access.

Source & status

Source

Health Canada

Tier

beta

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

81509

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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