- Recalling firm
- Medline Industries, LP
- Reason for recall
- Component labeling discrepancy
- Affected products (lot / model / serial)
- UDI/DI 10198459582158 (each) 40198459582159 (case), Lot Number 26FLA408
- Units affected
- 45 kits
- Distribution pattern
- US Nationwide distribution in the state of California.
- Firm location
- Northfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2999-2026
- Recall initiated
- July 10, 2026
- FDA classification date
- August 21, 2026
- FDA report date
- September 2, 2026
- FDA event ID
- 99506
- Last updated on HTM Vibe
- September 8, 2026