Quick Facts at a Glance
- Recall Date
- July 25, 2025
- Hazard Level
- HIGH
- Brand
- Medline Industries
- Category
- Health & Personal Care
- Sold At
- Unknown
- Geographic Scope
- 5 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
- Medline Industries
- Product type
- Fiber Optic Laryngoscope Handles
- Model numbers
- ACC010381C, ACC010532, ACC010671, ACC010728
- Sold at
- Unknown
- Where affected
- AL, CA, DE, TN, TX
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
July 25, 2025
Reported by FDA DEVICE
October 1, 2025
RecallRadar source check
April 18, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact MEDLINE INDUSTRIES, LP - Northfield or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
About This Product
Medline kits are used in medical settings to aid airway management. They include Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. These kits support clinicians during intubation.
Why This Is Dangerous
If the light in the laryngoscope handle does not illuminate, clinicians may have difficulty visualizing the airway. This could delay or complicate airway management.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Healthcare facilities may need to substitute devices or delay procedures. The risk is situational and depends on the urgency of airway management.
Practical Guidance
How to identify if yours is affected
- Check inventory for ACC010381C, ACC010532, ACC010671, ACC010728.
- Inspect laryngoscope handles to verify illumination.
- If affected, stop using and follow recall instructions.
Where to find product info
Model numbers are printed on kit labeling and packaging.
What timeline to expect
4-6 weeks for refunds or replacements typical in recalls.
If the manufacturer is unresponsive
- Escalate to FDA recall portal if Medline does not respond within 1-2 weeks
- Document all contact attempts and responses
How to prevent similar issues
- Verify recall status in supply chain before using devices
- Sign up for recall alerts from Medline and FDA
- Implement a recall workflow for airway equipment
Documentation advice
Keep copies of recall notices, model numbers, lot numbers, and all correspondence with Medline
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Product Details
Quick-reference: - ACC010381C NEWBORN RESUSCITATION KIT - ACC010532 DRAWER 5 - POSITION 3 - ACC010671 DRAWER #4C ADULT - ACC010728 DRAWER #2 Distribution: US distribution to AL, CA, DE, OR, TN, TX When sold: Unknown Price: Unknown
Reported Incidents
No injuries or incidents have been reported.
Key Facts
- Kits distributed in AL, CA, DE, OR, TN, TX
- Hazard: illumination failure of Flexicare BritePro Solo fiber optic handles
- Stop use immediately and follow recall instructions
- Remedy not specified in the notice; contact Medline for guidance
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Safety Guide
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