MEDLINE INDUSTRIES, LP - Northfield: Device Recall
Recall #Z-2567-2025 · 07/25/2025
Class I: Dangerous
Recall Details
- Recall Number
- Z-2567-2025
- Classification
- Class I
- Product Type
- Device
- Recalling Firm
- MEDLINE INDUSTRIES, LP - Northfield
- Status
- Ongoing
- Date Initiated
- 07/25/2025
- Location
- Northfield, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 596 units
Reason for Recall
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.
Product Description
Medline medical convenience kits labeled as: 1. NEWBORN RESUSCITATION KIT, Kit Number ACC010381C; 2. DRAWER 5 - POSITION 3, Kit Number ACC010532; 3. DRAWER #4C ADULT, Kit Number ACC010671; 4. DRAWER #2, Kit Number ACC010728.
Distribution Pattern
US distribution to: AL, CA, DE, OR, TN, TX
Other Recalls by MEDLINE INDUSTRIES, LP - Northfield
- Class I: Dangerous 07/25/2025
- Class II: Risk 07/23/2025
- Class I: Dangerous 07/14/2025
- Class II: Risk 07/08/2025
- Class II: Risk 07/07/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.