- Recalling firm
- Medline Industries, LP
- Reason for recall
- There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
- Affected products (lot / model / serial)
- UDI-DI: (CS) 40198459071455, (EA) 10198459071454; Lot Number: 25GBB924
- Units affected
- 420 units
- Distribution pattern
- US Nationwide distribution in the state of MN.
- Firm location
- Northfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1693-2026
- Recall initiated
- February 18, 2026
- FDA classification date
- March 27, 2026
- FDA report date
- April 8, 2026
- FDA event ID
- 98529
- Last updated on HTM Vibe
- July 24, 2026