RecallRadar

FDA Drug recall D-0542-2023

Dianeal Low Calcium (2.5 mEq/L) Peritonial Dialysis Solution with 1.5% Dextrose, packaged in a) 5000 mL per Ambu-Flex II Container bag, Pro…

On 2023-05-03 the FDA classified a Class II recall of Dianeal Low Calcium (2.5 mEq/L) Peritonial Dialysis Solution with 1.5% Dextrose, packaged in a) 5000 mL per Ambu-Flex II Container bag, Pro… by Baxter Healthcare, citing lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0542-2023
ClassificationClass II
Statuscompleted
Initiated2023-03-15
Published2023-05-03
Last updated2026-09-13 11:52 UTC
CompanyBaxter Healthcare
DistributionUS

Product

Dianeal Low Calcium (2.5 mEq/L) Peritonial Dialysis Solution with 1.5% Dextrose, packaged in a) 5000 mL per Ambu-Flex II Container bag, Product Code L5B4826, NDC 0941-0409-07; and b) 6000 mL per Ambu-Flex II Container bag, Product Code L5B9770, NDC 0941-0409-01, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA.

Reason

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

Identifiers

ndc0941-0411-05
ndc0941-0411-06
ndc0941-0411-07
ndc0941-0411-04
ndc0941-0411-11
ndc0941-0413-05
ndc0941-0413-06
ndc0941-0413-07
ndc0941-0413-01
ndc0941-0413-04
ndc0941-0415-05
ndc0941-0415-06
ndc0941-0415-04
ndc0941-0415-07
ndc0941-0415-01
ndc0941-0409-06
ndc0941-0409-05
ndc0941-0409-07
ndc0941-0409-01
ndc0941-0457-08
ndc0941-0457-02
ndc0941-0457-05
ndc0941-0457-01
ndc0941-0459-08
ndc0941-0459-02
ndc0941-0459-05
ndc0941-0459-01
ndc0941-0426-52
ndc0941-0426-53
ndc0941-0427-52
ndc0941-0427-53
ndc0941-0429-52
ndc0941-0429-53
ndc0941-0424-51
ndc0941-0424-52
ndc0941-0424-53
ndc0941-0430-51
ndc0941-0430-52
ndc0941-0430-53
ndc0941-0433-51
ndc0941-0433-52
ndc0941-0433-53
ndc0941-0484-01
ndc0941-0487-01
ndc0941-0490-01
code_infoLot #: a) Y406130, Exp 31-Oct-2024; b) Lots Y406314, Y406314A, Y406963, Y407199, Exp 31-Oct-2024

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: completed.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0542-2023%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.