HIGH

Medline Recalls 2,520 Kits With Flexicare Laryngoscope Handles Over Lighting Failure (2025)

Medline Industries, LP recalled 2,520 Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles sold to U.S. hospitals and healthcare facilities. The lights on the handles may fail to illuminate as intended. Hospitals should stop using the devices immediately and follow recall instructions.

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

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

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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

  1. Check kit labels for model numbers ACC010369B, ACC010379A, ACC010392, ACC010467A, ACC010469, ACC010480, ACC010480A, ACC010540, ACC010593A, ACC010593B, DYNDA1847A, DYNJAA245A.
  2. Confirm the kit is among the recalled Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles.
  3. 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.

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

  • 2520 units recalled
  • 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)

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTCHILDRENINFANTSPETS
Injury Types
ELECTRICALOTHER

Product Details

Brand
Model Numbers
ACC010369B
ACC010379A
ACC010392
ACC010467A
ACC010469
+7 more
Affected States
AL, CA, DE, TN, TX
Report Date
October 1, 2025
Recall Status
ACTIVE

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