Medline medical convenience kits labeled as: 1 — Class I medical device recall Z-2566-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-10-01, distributed in AL, CA, DE, OR, TN, TX. Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicar
| Recall number | Z-2566-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2025-07-25 |
| Classified | 2025-09-19 |
| Reported by FDA | 2025-10-01 |
| Distributed | AL, CA, DE, OR, TN, TX |
| Quantity | 2,520 units |
| UPC / GTIN / UDI-DI | 10193489218053, 10193489414677, 10193489481259, 10193489499933, 10193489777512, 10193489777529, 10193489804584, 10193489834550, 10193489977547, 10195327009366, 10195327168995, 10195327195472, 40193489218054, 40193489414678, 40193489481250, 40193489499934, 40193489777513, 40193489777520, 40193489804585, 40193489834551, 40193489977548, 40195327009367, 40195327168996, 40195327195473 |
| Lot numbers | ACC010379A, ACC010392, ACC010467A, ACC010469, ACC010480, ACC010480A, ACC010540, ACC010593A, ACC010593B, DYNDA1847A, DYNJAA245A |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2566-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.