FDAOctober 10, 2025device

DYNJ909119G ROBOTIC GASTRIC LAP SLEEVE-LF DYNJ909127F CYSTO DYNJ909129D GENERAL LAPAROSCOPY-LF

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

401984590554241019845905542340198459055264101984590552634019845913052710198459130526

Recall history

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

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