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Minicap with Povidone-Iodine Solution (2015-01-21)
- Starting date:
- January 21, 2015
- Posting date:
- January 30, 2015
- 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-43565
Recalled Products
Minicap with Povidone-Iodine Solution
Reason
Baxter has received complaints indicating that the sponge of the MINICAP was fully separated from the cap, partially protruding from the cap, or missing. Baxter Corporation is recalling seven (7) lots of MINICAP with povidone-iodine solution.
Affected products
Minicap with Povidone-Iodine Solution
Lot or serial number
- GD896837
- GD896845
- GD896944
- GD897124
- GD897157
- GD897165
- GD897371
Model or catalog number
5C4466P
Companies
- Manufacturer
-
Baxter Healthcare Corporation
1 Baxter Parkway
Deerfield
60015
Illinois
UNITED STATES