HIGH

Medline Recalls Intubation Trays Due to Light Failure Hazard

Medline Industries, LP recalled 2,520 medical convenience kits on July 25, 2025. The recall affects multiple intubation trays containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The light in these devices fails to illuminate, posing a serious risk in emergency situations.

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

Product Details

The recall includes the following kits: Adult Intubation Tray (ACC010369B), Adult ICU Intubation Tray (ACC010379A), and others. These kits were distributed across several states including California and Texas. They were sold for an estimated price of $200.

The Hazard

The affected laryngoscope handles in these kits fail to illuminate as intended. This malfunction can hinder emergency medical procedures, potentially leading to serious complications.

Reported Incidents

There have been no reported injuries or deaths related to this recall. However, the failure of these devices to function properly poses a high risk in critical care situations.

What to Do

Healthcare providers and patients should stop using the recalled kits immediately. Contact Medline Industries for further instructions and return information.

Contact Information

For questions, call Medline Industries at 1-800-633-5463 or visit their website at https://www.medline.com.

Key Facts

  • Recall date: July 25, 2025
  • Number of units recalled: 2,520
  • States affected: AL, CA, DE, OR, TN, TX
  • Hazard classification: Class I
  • Immediate action required
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Safety Assessment

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

Product Details

Model Numbers
ACC010369B
ACC010379A
ACC010392
ACC010467A
ACC010469
+7 more
Affected States
AL, CA, DE, TN, TX
Report Date
October 1, 2025
Source Agency
FDA - Medical Devices
Recall Status
ACTIVE
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