Recall Ledger

Sterile Radiology Procedure Kits recall (Medline Industries, LP)

Medical deviceClass IIOngoing

Summary: Medline Industries, LP is recalling Sterile Radiology Procedure Kits, Model Number DYNDH1491B. Reason: There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.

What is being recalled

Sterile Radiology Procedure Kits, Model Number DYNDH1491B

Why

There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide distribution in the state of MN. (states named: Minnesota)

How to tell if yours is affected

UDI-DI: (CS) 40198459071455, (EA) 10198459071454; Lot Number: 25GBB924

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-1693-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedFebruary 18, 2026
ReportedApril 8, 2026
CompanyMedline Industries, LP
Company locationNorthfield, IL, United States
Initiated byVoluntary: Firm initiated
Quantity420 units

More recalls from Medline Industries, LP · all medical device recalls · recalls from February 2026

Official FDA record