B BRAUN MEDICAL INC Recalls Lactated Ringer's Injection USP
This is a Class I recall — the most serious type. There is a reasonable probability of serious health consequences or death.
B BRAUN MEDICAL INC Recalls Lactated Ringer's Injection USP
B BRAUN MEDICAL INC · Class I — Most Serious

Product Description
Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07.
Reason for Recall
Presence of Particulate Matter.
FDA Classification
Class I — Most Serious
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.
Distribution
U.S.A. Nationwide
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
A Class I recall — the FDA's most urgent classification — has been issued for a pharmaceutical product recalled by B BRAUN MEDICAL INC on April 28, 2026. Presence of Particulate Matter. This recall affects 95,412 containers and was distributed in U.S.A. Nationwide. Class I recalls indicate a reasonable probability of serious health consequences or death. Consumers should stop using this product immediately.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medical Product Contamination.