FDAOctober 10, 2025device

Convenience kits; DYNJ901046M GYN ROBOTIC DYNJ909120D ROBOTIC PROSTATE

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment.

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lpmedlinemedline industries

UPCs

40198459130381101984591303804019845913054110198459130540

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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