Class II

Medical Device Recall: Sterile Radiology Procedure Kits, Model Number DYNDH1491B

Medline Industries, LP · February 18, 2026

Reason for Recall

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

Distribution

US Nationwide distribution in the state of MN.

States Affected

NATIONWIDE

Quantity Affected

420 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1693-2026

Status: ongoing

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