D-1593-2014 Class I Terminated

Recalled by Baxter Healthcare Corp. — Deerfield, IL

FDA drug recall D-1593-2014 was initiated by Baxter Healthcare Corp. on Jul 11, 2014 and is designated Class I. Reason for recall: Presence of Particulate Matter: particulate matter identified as fibers and/or plastics The recall status is terminated (terminated Sep 21, 2016). Affected quantity: 171,672 bags.

Recall Details

Product Type
Drugs
Report Date
Sep 24, 2014
Initiation Date
Jul 11, 2014
Termination Date
Sep 21, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
171,672 bags

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.

Reason for Recall

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

Distribution Pattern

Nationwide, Puerto Rico, Singapore, and Hong Kong

Code Information

Lot #: P309476, Exp 10/14

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-1593-2014
openFDA file date
Oct 27, 2026
Loaded by RegDataLab
Oct 29, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.