- Recalling firm
- Medline Industries, LP
- Reason for recall
- On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.
- Affected products (lot / model / serial)
- Medline Kit Number/SKU CIT7050F, UDI/DI each 10198459536656, UDI/DI case 40198459536657, Lot Number 25KLA002
- Units affected
- 640 kits
- Distribution pattern
- US Nationwide distribution in the state of South Carolina.
- Firm location
- Northfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1824-2026
- Recall initiated
- March 16, 2026
- FDA classification date
- April 16, 2026
- FDA report date
- April 22, 2026
- FDA event ID
- 98626
- Last updated on HTM Vibe
- July 24, 2026