FDA recall record

Potassium Chloride Injection, 20 mEq per 50 mL, 50 mL Sterile Single Dose Container bag recall — FDA D-1593-2014

Presence of Particulate Matter: particulate matter identified as fibers and/or plastics

Class Iclassification
D-1593-2014official record ID
Sep 24, 2014report date

Recall record at a glance

Official recordD-1593-2014
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmBaxter Healthcare Corp.
Report dateSep 24, 2014
Recall initiation dateJul 11, 2014
Quantity171,672 bags
LocationDeerfield, IL, United States

Official product description

Potassium Chloride Injection, 20 mEq per 50 mL, 50 mL Sterile Single Dose Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, NDC 0338-0703-41, Product Code 2B0822.

Why the product was recalled

Presence of Particulate Matter: particulate matter identified as fibers and/or plastics

Distribution information

Nationwide, Puerto Rico, Singapore, and Hong Kong

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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