This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
MiniCap Disconnect Cap
- Starting date:
- May 21, 2013
- Posting date:
- June 18, 2013
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-34227
Recalled products
- MiniCap Disconnect Cap
Reason
Baxter has received complaints for opened pouches of MiniCap contained within the shipping carton of product code 5C4466P (lot #GD893891). Baxter has determined the opened pouches were due to an incomplete seal. An incomplete seal may result in the povidone-iodine drying off within the Minicap and becoming an ineffective disinfectant.
Affected products
A. MiniCap Disconnect Cap
Lot or serial number
- GD893891
Model or catalog number
- 5C4466P
Companies
- Manufacturer
-
Baxter Healthcare Corporation
1 Baxter Parkway
Deerfield
60015
Illinois
UNITED STATES