RecallRadar

FDA Drug recall D-1593-2014

Potassium Chloride Injection, 20 mEq per 50 mL, 50 mL Sterile Single Dose Container bag, Rx only, Baxter Healthcare Corporation, Deerfield,…

On 2014-09-24 the FDA classified a Class I recall of Potassium Chloride Injection, 20 mEq per 50 mL, 50 mL Sterile Single Dose Container bag, Rx only, Baxter Healthcare Corporation, Deerfield,… by Baxter Healthcare, citing presence of Particulate Matter: particulate matter identified as fibers and/or plastics.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1593-2014
ClassificationClass I
Statusterminated
Initiated2014-07-11
Published2014-09-24
Last updated2026-09-13 11:51 UTC
CompanyBaxter Healthcare
DistributionUS

Product

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

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

Identifiers

ndc0338-0703-41
ndc0338-0703-48
ndc0338-0705-41
ndc0338-0705-48
ndc0338-0709-48
code_infoLot #: P309476, Exp 10/14

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1593-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.