Laerdal Medical recalled 1,202 Compact Suction Units on January 13, 2026. The recall affects models LCSU 4, 800 ml and LCSU 4, 300 ml due to excessive electromagnetic noise. Patients and healthcare providers must stop using the devices immediately.
units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter 21, Equipment Category M.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Laerdal Medical Corporation or your healthcare provider for instructions. Notification method: Letter
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The Laerdal Compact Suction Unit is a medical device used to clear airways in patients. Healthcare providers often use it in emergency situations to ensure patient safety during respiratory distress.
Excessive electromagnetic noise from the recalled units could disrupt the functioning of other medical equipment, posing a risk to patient safety.
This recall is not part of a broader industry pattern.
The recall urges immediate action from healthcare providers to prevent potential interference in patient care.
The model and catalog numbers are usually found on the device's label or packaging.
Expect a refund or replacement process to take approximately 4-6 weeks.
Document all correspondence related to the recall, including emails, letters, and any phone call notes.
The recalled models are LCSU 4, 800 ml (Catalog Number: 880052), LCSU 4, 300 ml (Catalog Number: 880062), and LCSU 4 (Catalog Number: 881152). These units were distributed worldwide, including the US, Denmark, Sweden, Norway, Canada, Finland, Australia, and several European countries. The devices were sold from 2021 to 2026.
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