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Soft-vu and accu-vu 4 fr angiographic catheters

Official notice

18 Mar 2026

Last checked

18 Mar 2026

Medium riskHealth Canada
Watch Angiodynamics

An official Health Canada notice concerns Soft-vu and accu-vu 4 fr angiographic catheters. AngioDynamics, Inc., is conducting a voluntary medical device field safety corrective action or recall to the end-user level based on the non-conformance of a molded hub in specific models and lots of Soft-Vu and Accu-Vu 4 fr angiographic catheters. The affected Soft-Vu and Accu-Vu 4 fr angiographic catheters being recalled (removed) contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. AngioDynamics has become aware of the non-conformance by way of multiple complaints associated with the affected angiographic catheter devices; however, there have been no complaints or events that occurred in Canada. There are no reports of patient injury as a result of this issue. Published 2026-03-18.

What to do now

Contact the manufacturer if you require additional information.

Recall number

81769

Official notice

2026-03-18

The hazard

AngioDynamics, Inc., is conducting a voluntary medical device field safety corrective action or recall to the end-user level based on the non-conformance of a molded hub in specific models and lots of Soft-Vu and Accu-Vu 4 fr angiographic catheters. The affected Soft-Vu and Accu-Vu 4 fr angiographic catheters being recalled (removed) contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. AngioDynamics has become aware of the non-conformance by way of multiple complaints associated with the affected angiographic catheter devices; however, there have been no complaints or events that occurred in Canada. There are no reports of patient injury as a result of this issue.

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

10714009, 10714016, 13709804, H787107100315, 10732301, 10714001, 10707103, 10714002, 10714018, 10714017, 10714021, 10714014, 10734301

Other

RA RA-81769

Model Numbers

10714009, 10714016, 13709804, H787107100315, 10732301, 10714001, 10707103, 10714002, 10714018, 10714017, 10714021, 10714014, 10734301

Recall Numbers

81769

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Affected products

Product 1

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10714009

Product 2

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10714016

Product 3

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 13709804

Product 4

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - H787107100315

Product 5

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10732301

Product 6

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10714001

Product 7

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10707103

Product 8

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10714002

Product 9

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10714018

Product 10

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10714017

Product 11

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10714021

Product 12

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10714014

Product 13

Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalogue number - 10734301

Risk / hazard

AngioDynamics, Inc., is conducting a voluntary medical device field safety corrective action or recall to the end-user level based on the non-conformance of a molded hub in specific models and lots of Soft-Vu and Accu-Vu 4 fr angiographic catheters. The affected Soft-Vu and Accu-Vu 4 fr angiographic catheters being recalled (removed) contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. AngioDynamics has become aware of the non-conformance by way of multiple complaints associated with the affected angiographic catheter devices; however, there have been no complaints or events that occurred in Canada. There are no reports of patient injury as a result of this issue.

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

Angiodynamics

Manufacturer

Not provided

Phone

Not provided

Brand: Angiodynamics.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

81769

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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