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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

Laerdal LCSU 4 RTCA Suction Units Recalled for Electromagnetic Noise

Agency Publication Date: February 11, 2026
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Summary

Laerdal Medical Corporation is recalling 1,202 units of the Laerdal Compact Suction Unit 4 (LCSU 4) RTCA version because they may emit electromagnetic noise beyond acceptable safety limits for aircraft environments. These portable medical suction devices, manufactured in the United States and distributed worldwide, include catalog numbers 880052, 880062, and 881152. Consumers should identify these products by checking the catalog and UDI-DI numbers on the device label and contact the manufacturer for further instructions.

Risk

The device can emit excessive electromagnetic interference which may disrupt the navigation or communication systems of an aircraft during flight. This interference could potentially lead to safety hazards for the aircraft and its passengers.

What You Should Do

  1. Check your device label to see if you have an affected Laerdal Compact Suction Unit 4 (LCSU 4) RTCA version with Catalog Numbers 880052, 880062, or 881152.
  2. Verify the UDI-DI on your device matches 07045432088519, 07045432088533, or 07045432067132.
  3. Stop using the recalled device for aircraft applications immediately.
  4. Contact Laerdal Medical Corporation or your distributor to arrange for a return, replacement, or correction of the unit.
  5. Call the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls for more information regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Laerdal Compact Suction Unit 4 RTCA version (LCSU 4 RTCA)
Variants: 800 ml, 300 ml
Model / REF:
880052
880062
881152
UDI:
07045432088519
07045432088533
07045432067132

Units manufactured in a limited time period may emit electromagnetic noise beyond acceptable limits for RTCA application.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98039
Status: Active
Manufacturer: Laerdal Medical Corporation
Sold By: Direct from manufacturer; Medical equipment distributors
Manufactured In: United States
Units Affected: 1202 units (537 US, 665 OUS) (2/23/2026: 574 US, 1239 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.