FDA Drug Recalls

Recalls / Class II

Class IID-1141-2023

Product

Dianeal PD-2 Peritonial Dialysis Solution with 1.5% Dextrose, 5000 mL AMBU-FLEX ll Container with yellow pull ring, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA Product code L5B5193 NDC 0941-0411-07

Brand name
Dianeal Low Calcium With Dextrose
Generic name
Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride And Dextrose
Active ingredients
Calcium Chloride, Dextrose Monohydrate, Magnesium Chloride, Sodium Chloride, Sodium Lactate
Route
Intraperitoneal
NDCs
0941-0409, 0941-0411, 0941-0413, 0941-0415, 0941-0457, 0941-0459, 0941-0426, 0941-0427, 0941-0429, 0941-0424 +5 more
FDA application
NDA017512
Affected lot / code info
Lot Y406734, Exp 31-Oct-2024

Why it was recalled

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

Recalling firm

Firm
Baxter Healthcare Corporation
Manufacturer
Vantive US Healthcare LLC
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1 Baxter Pkwy, N/A, Deerfield, Illinois 60015-4625

Distribution

Quantity
22,112 bags
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2023-08-11
FDA classified
2023-08-29
Posted by FDA
2023-09-06
Terminated
2024-07-16
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1141-2023. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: Dianeal Low Calcium With Dextrose · FDA Drug Recalls