SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number… recallZ-0921-2026 · Medline Industries, LP · initiated Nov 13, 2025

Open, Classified

Is my device affected?

Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
If yours is listed, follow the instructions from Medline Industries, LP or your healthcare provider. The company's action is summarized under what the company is doing.
Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was 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.

FDA root cause category: Packaging process control

What the company is doing

An URGENT MEDICAL DEVICE RECALL notification letter dated 11/13/25 was sent to customers. REQUIRED ACTION: 1. Immediately check your stock for the affected item number(s) and the affected lot number(s) listed on the enclosed response form. Quarantine all affected product. Upon completion of the below actions, please destroy affected product. 2. Please complete and return the enclosed response form listing the quantity of affected product you have in inventory. Even if you do not have any affected product in inventory, please complete and return the response form. 3. Your account will receive credit once the response form is submitted, if applicable. 4. If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please request that customers destroy any affected product. You should include your customers quantities on your response form. If you have any questions, contact the Recall Department at 866-359-1704 or [email protected].

Recall details

Recall number: Z-0921-2026
Status: Open, Classified
Initiated by the company: Nov 13, 2025
Posted by the FDA: Dec 12, 2025
Recalling firm: Medline Industries, LP
Quantity: 56 units
Product code: LRW
Distribution: US Nationwide distribution in the states CA, CO, IL, KS, and MI.

Product description

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

Code information (models, lots, serial numbers)

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

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

MEDLINE DYND04000
Medline Industries, Inc. · SCISSORS, GENERAL, SURGICAL
3 recalls0 reports

Other products in the same recall event

The FDA groups related products into one recall event (event 98066).

Z-0922-2026 · Open, Classified
FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048

Sources and updates

Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.

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