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

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  Reason
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  Affected products

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