Health product recall

Minicap Disconnect Cap With Povidone-Iodine

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
GD912143
GD912051
GD912099

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