# FDA recall Z-2566-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class I · device recall initiated 2025-07-25.

## Product

Medline medical convenience kits labeled as:    1. ADULT INTUBATION TRAY, Kit Number ACC010369B;   2. ADULT ICU INTUBATION TRAY, Kit Number ACC010379A;   3. INTUBATION TRAY, Kit Number ACC010392;   4. INTUBATION KIT, Kit Number ACC010467A;   5. ADULT AIRWAY TRAY, Kit Number ACC010469;   6. TRAY 2 INTUBATION DRAWER, Kit Number ACC010480;   7. TRAY 2 INTUBATION DRAWER, Kit Number ACC010480A;   8. ADULT INTUBATION, Kit Number ACC010540;   9. DIFFICULT AIRWAY TRAY #1, Kit Number ACC010593A;   10. DIFFICULT AIRWAY TRAY #1, Kit Number ACC010593B;   11. INTUBATION TRAY, Kit Number DYNDA1847A;   12. INTUBATION TRAY (ADULT), Kit Number DYNJAA245A.

## 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.

## Distribution

US distribution to:  AL, CA, DE, OR, TN, TX

## Key facts

- **Recall number:** Z-2566-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-25
- **Report date:** 2025-10-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2566-2025

## Citation

> AI Analytics. FDA recall Z-2566-2025. Retrieved 2026-08-23 from https://api.ai-analytics.org/recall/Z-2566-2025. Source: US FDA. Licensed CC0.

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