B Braun Medical Inc: Lactated Ringer's Injection Usp

Recall Summary B. Braun Medical Inc. is recalling Lactated Ringer's Injection USP in 1000 mL containers nationwide because the solution contains particulate matter (small particles). This intravenous fluid was distributed across all U.S. states and the District of Columbia. The recall affects prescription-only product with NDC number 0264-7750-07 manufactured by B. Braun Medical, Inc. in Bethlehem, Pennsylvania.

Recalling firm
B BRAUN MEDICAL INC
Product
Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07.
Reason
Presence of Particulate Matter.
Category
drug recall
Country
United States
Agency
U.S. Food and Drug Administration
Recall date
2026-04-28
Status
Ongoing
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
U.S.A. Nationwide

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/d2c4d77f-9613-43ba-be2c-08c2d8b00fd2