Medical device recalls High risk

MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical convenience kits labeled as: 1. NEWBORN RESUSCITATION KIT, Kit Number ACC010381C; 2. DRAWER 5 - POSITIO…

Recall date
July 25, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2567-2025
FDA classification
Class I
Brand / firm
MEDLINE INDUSTRIES, LP - Northfield
Sold / distributed
US distribution to: AL, CA, DE, OR, TN, TX

Why it was recalled

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.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

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.

Get recall alerts

Free email alert whenever MEDLINE INDUSTRIES, LP - Northfield has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: MEDLINE INDUSTRIES, LP - Northfield