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FDA · DrugsClass I

B Braun Medical Inc drug recall: Lactated Ringer's Injection USP

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Drugs
Classification
Class I
Status
Ongoing
Event ID
98795
Recall initiated
Apr 28, 2026
Classified by FDA
May 18, 2026
Posted in Enforcement Report
May 13, 2026
Recalling firm
B BRAUN MEDICAL INC
Firm location
Allentown, PA, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Press Release
Products in this event
1

What to do

Compare the product, lot or serial numbers below with what you have. If you use a prescription drug or medical device in this recall, talk to your pharmacist or health care provider before you stop using it, and follow the firm's instructions.

View the official FDA record ↗

Reason for recall

Presence of Particulate Matter.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Apr 28, 2026. FDA classified it 20 days later, on May 18, 2026. Distribution reported by FDA: U.S.A. Nationwide B BRAUN MEDICAL INC has 91 recalls in our records.

Recalled products (1)

  • D-0540-2026 Class I Ongoing

    Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07.

    Codes / lots: Lot #:J4P756, J4S843, Exp 5/31/2027

    Quantity: 95,412 containers

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA drug enforcement dataset
Official notice
FDA Enforcement Report, event 98795
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.

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