Health product recall

Medline convenience kits containing Namic Angiographic Manifolds

Last updated

Summary

Product
Medline convenience kits containing Namic Angiographic Manifolds
Issue
Medical devices - Performance
What to do

Customers are directed to remove and destroy all manifolds. Over-labels will be provided for any affected kits on hand stating that the affected manifolds must be removed and discarded from further use.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Namic Convenience Kit

103572

60716233

Namic Convenience Kit

140414

60716233

Namic Convenience Kit

187932

60716233

Namic Convenience Kit

107115

60701816

Namic Convenience Kit

110268

60701816

Namic Convenience Kit

97460

60780115

Namic Convenience Kit

103526

60780115

Namic Convenience Kit

104349

60780115

Namic Convenience Kit

106356

60780115

Namic Convenience Kit

107916

60780115

Namic Custom Angiographic Kit

More than 10 numbers, contact manufacturer.

60701103

Namic Custom Angiographic Kit

More than 10 numbers, contact manufacturer.

60701152

Clot Retrieval Pack

26CBE251

DYNJ56140C

Clot Retrieval Pack

26ABK843

DYNJ56140C

Clot Retrieval Pack

25HBV231

DYNJ56140C

Issue

Medline Industries is issuing a recall for specific item(s) and lot(s) of Medline convenience kits that contain Namic Angiographic Star Off Handle Manifolds.  Medline has identified the presence of particulate within the fluid path of the manifolds. Particulate within the manifold fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels. This carries a risk of serious injury, such as tissue or organ ischemia, or death.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Neurology
Health products - Medical devices - Cardiovascular
Health products - Medical devices - General and plastic surgery
Companies

Medline Industries, LP

Three Lakes Drive, Northfield, Illinois, United States, 60093

Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Recall date
Identification number
RA-82026

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