Data Foundry

Medical device recalls 2025

Medline medical convenience kits labeled as: 1 — Class I medical device recall Z-2567-2025

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 numberZ-2567-2025
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States
Recall initiated2025-07-25
Classified2025-09-19
Reported by FDA2025-10-01
DistributedAL, CA, DE, OR, TN, TX
Quantity596 units
UPC / GTIN / UDI-DI10193489902358, 10193489922127, 10195327351090, 10195327506544, 40193489902359, 40193489922128, 40195327351091, 40195327506545
Lot numbersACC010532, ACC010671, ACC010728

Product

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.

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-2567-2025. 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.