Data Foundry

Drug recalls 2014

Clinimix 4 — Class I drug recall D-1158-2014

Terminated recall by Baxter Healthcare Corp., reported 2014-03-26, distributed nationwide. Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.

Recall numberD-1158-2014
Product typeDrug
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBaxter Healthcare Corp., Deerfield, IL, United States
Recall initiated2013-11-18
Classified2014-03-14
Reported by FDA2014-03-26
Terminated2016-09-20
DistributedNationwide (US)
Quantity14,574 bags
Reason classesspecification failure
NDC00338-0202, 00338-0202-01, 00338-0202-06, 00338-0206, 00338-0206-01, 00338-0206-04, 00338-0210, 00338-0210-01, 00338-0210-06, 00338-0214, 00338-0214-01, 00338-0214-04, 00338-1113, 00338-1113-04, 00338-1115, 00338-1115-04, 00338-1123, 00338-1123-04, 00338-1125, 00338-1125-04, 00338-1142, 00338-1142-03, 00338-1144, 00338-1144-03, 00338-1145 and 32 more
Lot numbersP287045
Expiration dates2014-06

Product

Clinimix 4.25/25 sulfite-free (4.25% Amino Acid in 25% Dextrose) Injection, 1000 mLCLARITY Dual Chamber Container bag, Rx only. Dist: Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015. NDC: 0338-1115-04.

Reason for recall

Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.

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-1158-2014. 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.