Remipack (2018-03-28)
- Starting date:
- March 28, 2018
- Posting date:
- April 6, 2018
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type I
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-66376
Affected products
Remipack
Reason
Janssen Inc. is initiating a recall of one lot of Remipack Baxter Corporation has issued a Type I Drug recall with respect to their 250ml Sodium Chloride injection bag (Product Code Jb1322p, Lot W7i05c2) which is contained in the noted lot of Remipack. There may be a potential for the solution bag to leak into the over-pouch, with the risk for contamination of the solution or of air entering the fluid path.
Affected products
Remipack
Lot or serial number
130897
Model or catalog number
S17721564
Companies
- Manufacturer
-
Janssen Inc.
19 Greenbelt Drive
Toronto
M3C 1L9
Ontario
CANADA