Medline Industries, LP: Device Recall

Recall #Z-0921-2026 · 11/13/2025

Class II: Risk

Recall Details

Recall Number
Z-0921-2026
Classification
Class II
Product Type
Device
Recalling Firm
Medline Industries, LP
Status
Ongoing
Date Initiated
11/13/2025
Location
Northfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
56 units

Reason for Recall

The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.

Product Description

SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000

Distribution Pattern

US Nationwide distribution in the states CA, CO, IL, KS, and MI.

Other Recalls by Medline Industries, LP

View all recalls by Medline Industries, LP →

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.