Data Foundry

Drug recalls 2023

DIANEAL Low Calcium — Class II drug recall D-1140-2023

Terminated recall by Baxter Healthcare Corporation, reported 2023-09-06, distributed nationwide. Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

Recall numberD-1140-2023
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBaxter Healthcare Corporation, Deerfield, IL, United States
Recall initiated2023-08-11
Classified2023-08-29
Reported by FDA2023-09-06
Terminated2024-07-16
DistributedNationwide (US)
Reason classessterility, packaging
NDC00941-0409, 00941-0409-01, 00941-0409-05, 00941-0409-06, 00941-0409-07, 00941-0411, 00941-0411-04, 00941-0411-05, 00941-0411-06, 00941-0411-07, 00941-0411-11, 00941-0413, 00941-0413-01, 00941-0413-04, 00941-0413-05, 00941-0413-06, 00941-0413-07, 00941-0415, 00941-0415-01, 00941-0415-04, 00941-0415-05, 00941-0415-06, 00941-0415-07, 00941-0424, 00941-0424-51 and 35 more
Lot numbers408790, Y403740, Y403740A, Y403948, Y405638, Y405805, Y406277, Y407304, Y407304A, Y407717, Y407717A, Y408554, Y420075
Expiration dates2024-09-30, 2024-10-31, 2024-11-30, 2025-04-30

Product

DIANEAL Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution 1.5% Dextrose, packaged in a) 2000 mL AMBU-FLEX II Container bag, Product Code L5B4825, NDC 0941-0409-06; b) 5000 mL AMBU-FLEX II Container bag, Product Code L5B4826, NDC 0941-0409-07; and c) 6000 mL AMBU-FLEX II Container bag, Product Code L5B9770, NDC 0941-0409-01, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA.

Reason for recall

Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

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-1140-2023. 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.