Quick Facts at a Glance
- Recall Date
- January 13, 2026
- Hazard Level
- HIGH
- Brand
- Laerdal Medical
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Laerdal Medical
- Product type
- Suction Unit
- Model numbers
- 1) LCSU 4, 800 ml, RTCA, Catalog Number: 880052, UDI-DI: 07045432088519, 2) LCSU 4, 300 ml, Catalog Number: 880062 +4 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
January 13, 2026
Reported by FDA DEVICE
February 18, 2026
RecallRadar source check
February 25, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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.
What You Should Do
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
About This Product
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.
Why This Is Dangerous
Excessive electromagnetic noise from the recalled units could disrupt the functioning of other medical equipment, posing a risk to patient safety.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall urges immediate action from healthcare providers to prevent potential interference in patient care.
Practical Guidance
How to identify if yours is affected
- Check the model and catalog number on your suction unit.
- Verify if your unit matches the recalled models: LCSU 4, 800 ml, Catalog Number 880052 or LCSU 4, 300 ml, Catalog Number 880062.
- Contact your healthcare provider if unsure about the product's status.
Where to find product info
The model and catalog numbers are usually found on the device's label or packaging.
What timeline to expect
Expect a refund or replacement process to take approximately 4-6 weeks.
If the manufacturer is unresponsive
- Keep a record of all communications with Laerdal Medical.
- Consider reaching out to consumer protection agencies for assistance.
How to prevent similar issues
- Ensure future medical devices comply with electromagnetic interference standards.
- Research the manufacturer's safety record before purchase.
- Look for devices with FDA approval and certifications.
Documentation advice
Document all correspondence related to the recall, including emails, letters, and any phone call notes.
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Product Details
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.
Key Facts
- Excessive electromagnetic noise risk
- No reported injuries or incidents
- Immediate stop-use notice issued
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Safety Guide
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