FDA Medical devices recall ·
Sterile Radiology Procedure Kits, Model Number DYNDH1491B recall
- Recall number
- Z-1693-2026
- Date
- (initiated February 18, 2026)
- Company / brand
- Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 420 units
- Hazard tags
- Sterility
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Why was it recalled?
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI-DI: (CS) 40198459071455, (EA) 10198459071454; Lot Number: 25GBB924
Distribution
US Nationwide distribution in the state of MN.
States: Minnesota
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1693-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.