Recall Z-0921-2026— Medline Industries, LP

Name: FDA recall Z-0921-2026
Creator: U.S. Food and Drug Administration
Published: 2025-11-13

Class II · Ongoing

Class II FDA medical device recall by Medline Industries, LP, initiated 2025-11-13. FDA's recall record names no specific 510(k) clearance for this event. Product: SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000. Reason: 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..

Recalling firm: Medline Industries, LP
Classification: Class II
Status: Ongoing
Initiated: 2025-11-13
Firm location: Northfield, IL, United States

Product description

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

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.