Startseite/Alle Rückrufe/FDA-D-0495-2026
FDA DrugsClass II

Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 18018-3524, NDC: 0264-7385-60.

Veröffentlicht: 29. April 2026Rückruf-ID: D-0495-2026Kategorie: Arzneimittel & MedikamenteLand: Vereinigte Staaten
US
PharmaceuticalFDA DrugsUSUS

Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 18018-3524, NDC: 0264-7385-60.

Recalling Firm: B BRAUN MEDICAL INC

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Mitteilung übersetzenTranslate notice text, hazard warnings, and descriptions into any supported language.

Grund für den Rückruf / Gefahr

Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.

Produktbeschreibung & Identifikation

Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 18018-3524, NDC: 0264-7385-60.

Additional Source Details

FieldValue
CityAllentown
StatePA
Openfda › Unii059QF0KO0R
Openfda › RouteINTRAVENOUS
Openfda › Spl ided933e44-2560-495b-879c-99c6a0bf8ba0
Openfda › Brand nameSTERILE WATER
Openfda › Spl set id8924e52e-8622-4ed6-a061-1908183e0a18
Openfda › Package ndc › 10264-7385-50
Openfda › Package ndc › 20264-7385-60
Openfda › Product ndc0264-7385
Openfda › Generic nameWATER
Openfda › Product typeHUMAN PRESCRIPTION DRUG
Openfda › Substance nameWATER
Openfda › Manufacturer nameB. Braun Medical Inc.
Openfda › Application numberNDA019633
Openfda › Is original packagertrue
Event id98693
Address 1861 Marcon Blvd
Address 2N/A
Code infoLot # J5H165, Exp Date: 31 May2028; Lot # J5E237, Exp Date: 30APR2028.
Postal code18109-9577
Report date20260429
Product typeDrugs
Product quantity24,928 bags
Reason for recallLack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260402
Initial firm notificationLetter
Center classification date20260428

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Drugs).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 1...?

Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (FDA Drugs). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Übersicht

  • Rückrufendes UnternehmenB BRAUN MEDICAL INC
  • StatusOngoing
  • RisikostufeClass II
  • DistributionUS Nationwide.
Recall Hazard Severity
High Alert (Class I)
Offizielle Behördenwarnung

📢 Warnung teilen

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🚨 SAFETY ALERT: B BRAUN MEDICAL INC - Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 18018-3524, NDC: 0264-7385-60.

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