Recall Z-1693-2026— Medline Industries, LP
Class II · Ongoing
Class II FDA medical device recall by Medline Industries, LP, initiated 2026-02-18. FDA's recall record names no specific 510(k) clearance for this event. Product: 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..
- Recalling firm
- Medline Industries, LP
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-02-18
- Firm location
- Northfield, IL, United States
Product description
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Reason for recall
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
Data sourced from openFDA. This site is unofficial and independent of the FDA.