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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