HIGHFDA DEVICE

Medline Recalls 596 Flexicare BritePro Solo Fiber Optic Laryngoscope Handles in 2025

Medline Industries, LP recalled 596 Medline kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The light may fail to illuminate as designed. Healthcare providers should stop using the devices immediately and follow recall instructions.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
July 25, 2025
Status
ACTIVE
Severity
8/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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.

  1. Recall announced

    July 25, 2025

  2. Reported by FDA DEVICE

    October 1, 2025

  3. RecallRadar source check

    April 18, 2026

  4. 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

  1. Check inventory for ACC010381C, ACC010532, ACC010671, ACC010728.
  2. Inspect laryngoscope handles to verify illumination.
  3. 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

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

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

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

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

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

Product Details

Model Numbers
ACC010381C
ACC010532
ACC010671
ACC010728
Affected States
AL, CA, DE, TN, TX
Report Date
October 1, 2025
Recall Status
ACTIVE

Related Recalls