Dextrose Solution
FDA Recall NDC 0264-7387
FDA Enforcement Report: View Recall Date, Reasons, and Safety Status
Active & Historical Enforcement Reports
The FDA has identified 1 recorded enforcement report(s) associated with Dextrose (NDC 0264-7387). A significant event, classified as Class II, was initiated on Apr 02, 2026 by B. Braun Medical Inc.. The reported reason for this action was: "Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed."
This recall is currently ONGOING. Healthcare providers and patients are advised to check their inventory immediately against the affected codes provided below.
This recall is currently ONGOING. Healthcare providers and patients are advised to check their inventory immediately against the affected codes provided below.
Reported Recall Events
April 2026 Class II Recall: Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Recall Number
Class II Ongoing
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Apr 02, 2026
Apr 29, 2026
17,124 bags
Recall Profile & Regulatory Data
Event ID
98693
Classification
Class II
Enforcement Status
Ongoing
Recalling Firm
B BRAUN MEDICAL INC
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
US Nationwide.
Product Description
DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7387-50.
Batch or Lot Expiration Information
Lot# J5H166, J5H167, Exp Date: 30NOV2026.
Affected Packages Involved in this Recall
0264-7387-50Product
About FDA Recall Enforcement Reports
FDA recall data documents classified recall actions associated with a product. Most recalls are limited to specific lots, batches, or package configurations rather than every unit of a drug.
If a recall is listed for an NDC, review the affected lot information and package details carefully. Patients and healthcare professionals should confirm whether a specific product in hand matches the lot or package information before assuming it is affected.
