April 2026 FDA Recall Lactated Ringers by B Braun Medical Inc
D-0540-2026 - Presence of Particulate Matter.

This Class I drug recall was voluntarily initiated by B Braun Medical Inc on April 28, 2026 for the product Lactated Ringers. The FDA reported the reason for recall as presence of particulate matter.. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0540-2026

Reason for Recall
Presence of Particulate Matter.
Initiated
04-28-2026
Reported
05-13-2026
Quantity
95,412 containers

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
98795
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class I - is a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Ongoing
Recalling Firm About Recalling Firm
The firm responsible for the recall.
B BRAUN MEDICAL INC
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Press Release
Distribution Pattern About Distribution Pattern
General area of initial distribution.
U.S.A. Nationwide
Product Description About Product Description
Full technical description of the product.
Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07.

Batch or Lot Expiration Information

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

Affected Packages Involved in this Recall

0264-7750-07 Lactated Ringers