Quick Facts at a Glance
- Recall Date
- July 25, 2025
- Hazard Level
- HIGH
- Brand
- Medline
- Category
- Health & Personal Care
- Sold At
- Unknown
- Geographic Scope
- 5 states
- At-Risk Groups
- GENERAL, PREGNANT, CHILDREN
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
- Product type
- Fiber Optic Laryngoscope Handle
- Model numbers
- ACC010369B, ACC010379A, ACC010392, ACC010467A, ACC010469, ACC010480, ACC010480A, ACC010540 +4 more
- 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 with Flexicare BritePro Solo Fiber Optic Laryngoscope Handles are used in airway management during procedures. They are intended for use by trained clinicians in hospital settings.
Why This Is Dangerous
If the light fails to illuminate, clinicians may not be able to visualize the airway properly, increasing risk during intubation.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
In hospital settings, a non-illuminating laryngoscope handle could delay airway management and compromise patient safety.
Practical Guidance
How to identify if yours is affected
- Check kit labels for model numbers ACC010369B, ACC010379A, ACC010392, ACC010467A, ACC010469, ACC010480, ACC010480A, ACC010540, ACC010593A, ACC010593B, DYNDA1847A, DYNJAA245A.
- Confirm the kit is among the recalled Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles.
- Inspect for any lighting issue during routine checks.
Where to find product info
Model numbers are printed on the label of each kit. The FDA recall page linked in the notice provides the official scope and instructions.
What timeline to expect
4-8 weeks for refunds or replacements after submission of required documentation.
If the manufacturer is unresponsive
- Document attempts to contact Medline and recall coordinators.
- Escalate to your hospital's purchasing or risk management department.
- If necessary, file a complaint with FDA recall contacts or your local health authority.
How to prevent similar issues
- Verify model numbers before procurement to avoid recalled lots.
- Stay updated with FDA recall pages and hospital recall communications.
- Require vendors to provide explicit confirmation that new stock is not recall-impacted.
Documentation advice
Keep copy of recall notice, photos of kit labels, purchase orders, and all correspondence with Medline or vendors.
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Product Details
Model numbers included in this recall: ACC010369B, ACC010379A, ACC010392, ACC010467A, ACC010469, ACC010480, ACC010480A, ACC010540, ACC010593A, ACC010593B, DYNDA1847A, DYNJAA245A. Distribution: US across AL, CA, DE, OR, TN, TX. Quantity recalled: 2520 units. Sold to: hospitals and healthcare facilities in the United States. Price information: Unknown.
Reported Incidents
No injuries or incidents have been reported.
Key Facts
- Models include ACC010369B, ACC010379A, ACC010392, ACC010467A, ACC010469, ACC010480, ACC010480A, ACC…
- DYNDA1847A, DYNJAA245A
- Distribution to AL, CA, DE, OR, TN, TX
- Class I recall (high risk)
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Safety Guide
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