Data Foundry

Drug recalls 2014

Clinimix 5/15 sulfite-free — Class I drug recall D-1160-2014

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-1160-2014
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)
Quantity7,388 bags
Reason classesspecification failure
NDC00338-0180, 00338-0180-01, 00338-0180-06, 00338-0184, 00338-0184-01, 00338-0184-04, 00338-0188, 00338-0188-01, 00338-0188-06, 00338-0194, 00338-0194-01, 00338-0194-04, 00338-0198, 00338-0198-01, 00338-0198-06, 00338-1089, 00338-1089-04, 00338-1091, 00338-1091-04, 00338-1099, 00338-1099-04, 00338-1101, 00338-1101-04, 00338-1133, 00338-1133-03 and 30 more
Lot numbersP285122
Expiration dates2014-05

Product

Clinimix 5/15 sulfite-free (5% Amino Acid in 15% Dextrose) Injection, 2000 mL CLARITY Dual Chamber Container bag, Rx only. Dist: Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015. NDC: 0338-1099-04.

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-1160-2014. 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.