Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hamilton G5 with software version between v2.41 Recalled by Hamilton Medical, Inc. Due to After performing the suctioning maneuver, including disconnecting the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hamilton Medical, Inc. directly.
Affected Products
Hamilton G5 with software version between v2.41, v2.42, v2.50. Catalog number: 1590001 and 1590002. Anesthesiology: Hamilton G5 ventilator is designed for intensive care ventilation of adult and pediatric patients, and optionally infants and neonatal patients. The device is intended for use in the hospital and institutional environment where health care professionals provide patient care.
Quantity: 1115
Why Was This Recalled?
After performing the suctioning maneuver, including disconnecting the patient, suctioning , and reconnecting the patient, the preset pattern of ventilation many not continue as expected.
Where Was This Sold?
US distribution only.
About Hamilton Medical, Inc.
Hamilton Medical, Inc. has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report