Data Foundry

Drug recalls 2014

5% Dextrose Injection — Class I drug recall D-1162-2014

Terminated recall by Baxter Healthcare Corp., reported 2014-03-26, distributed nationwide. Presence of Paticulate Matter; Baxter is issuing a voluntary recall for these IV solutions due to particulate

Recall numberD-1162-2014
Product typeDrug
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBaxter Healthcare Corp., Deerfield, IL, United States
Recall initiated2013-11-21
Classified2014-03-14
Reported by FDA2014-03-26
Terminated2016-09-21
DistributedNationwide (US)
Countries outside the USAE, SA, SG
Quantity105,216 containers
Reason classesspecification failure
NDC00338-0017, 00338-0017-02, 00338-0017-03, 00338-0017-04, 00338-0017-10, 00338-0017-11, 00338-0017-18, 00338-0017-31, 00338-0017-38, 00338-0017-41, 00338-0017-48, 00338-0023, 00338-0023-02, 00338-0023-03, 00338-0023-04
Lot numbers11/13, P285288

Product

5% Dextrose Injection, USP, 100 mL Single dose VIAFLEX plastic containers, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product code 2B0089, NDC 0338-0017-38.

Reason for recall

Presence of Paticulate Matter; Baxter is issuing a voluntary recall for these IV solutions due to particulate matter found in the solution identified as polyester and cotton fibers, adhesive-like mixture, polyacetal particles, thermally degraded PVC, black polypropylene and human hair embedded in the plastic bag

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1162-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.