Z-0921-2026Class II

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

Name: Z-0921-2026 SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Creator: Medline Industries, LP
Published: 2025-11-13
License: https://open.fda.gov/license/

MEDLINE INDUSTRIES, LP - Northfield / initiated 2025-11-13 / Open, Classified / root cause: packaging

FDA source

Medline Industries, LP began a recall of SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000 on 2025-11-13. FDA classified it as Class II and gives the reason as "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". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0921-2026
Classification: Class II
Status: Open, Classified
Initiated: 2025-11-13
Posted: 2025-12-12
Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product: SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Product code: LRW Scissors, General, Surgical
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.
Root cause tag: packaging
FDA root cause: Packaging process control
Action: 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].
Quantity in commerce: 56 units
Distribution: US Nationwide distribution in the states CA, CO, IL, KS, and MI.
Product codes and lots: DYND04000, UDI-DI: 10193489191349(each), 20193489191346(case), Lot Number: 2023102590

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0921-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0921-2026	Class II	Ongoing	Voluntary: Firm initiated	2025-12-24	2025-12-12
Z-0922-2026	Class II	Ongoing	Voluntary: Firm initiated	2025-12-24	2025-12-12

Product code LRW

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)