Minicap Disconnect Cap With Povidone-Iodine
Brand(s)
Last updated
Summary
Product
Minicap Disconnect Cap With Povidone-Iodine
Issue
Medical devices - Labelling and packaging
What to do
Contact the manufacturer if you require additional information.
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Minicap Disconnect Cap With Povidone-Iodine |
GD912112 |
5C4466P |
Issue
Baxter Corportation is issuing a recall for certain lots of the Minicap. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals.
Recall start date: February 01, 2023
Additional information
Details
Original published date: 2023-02-08
Alert / recall type
Health product recall
Category
Health product - Medical device - General hospital and personal use
Companies
Baxter Healthcare Corporation
1 Baxter Parkway, Deerfield, Illinois, United States, 60015
Published by
Health Canada
Audience
General public
Healthcare
Recall class
Type I
Identification number
RA-72674