FDAClass IIDecember 24, 2025

Scissors recall: Sterility Concern

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

Why was Scissors recalled?

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.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

DYND04000, UDI-DI: 10193489191349(each), 20193489191346(case), Lot Number: 2023102590

Product
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Recalling firm
Medline Industries, LP
Quantity
56 units
Distribution
US Nationwide distribution in the states CA, CO, IL, KS, and MI.
Recall date
December 24, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls