Salem Sump™ products
Brand(s)
Last updated
Summary
Product
Salem Sump™ products
Issue
Medical devices - Labelling and packaging
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| Salem Sump™ Dual Lumen Stomach Tube Anti-Reflux Valve | All lots. | 8888266122 8888266148 8888266130 8888266114 |
| Argyle™ PVC Salem Sump™ | All lots. | 8888264960 8888264986 8888264945 8888264929 |
Issue
Cardinal Health has created an electronic instruction for use (eIFU) for Salem Sump™ products because of reports of breakage in the ARV due to improper use of the device. These changes to the labeling have been made to increase user awareness of how to use the ARV correctly and to inform users of the new warning. Lots manufactured after May 1, 2019 are affected.
Recall start date: July 22, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Gastroenterology and urology
Companies
Cardinal Health Canada
1000 Tesma Way, Vaughan, Ontario, Canada, L4K 5R8
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75939
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