- Recalling firm
- LeMaitre Vascular, Inc.
- Reason for recall
- Labeling mix-up resulting in the incorrect lot outer packaging of product.
- Affected products (lot / model / serial)
- REF#: AG740; UDI-DI: 00316837000299; Serial Number: 24GG298-022; Expiration Date: 28Jun2027;
- Units affected
- 1 unit
- Distribution pattern
- US Nationwide distribution in the state of IL.
- Firm location
- North Brunswick, NJ, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1574-2026
- Recall initiated
- February 10, 2026
- FDA classification date
- March 19, 2026
- FDA report date
- March 25, 2026
- FDA event ID
- 98409
- Last updated on HTM Vibe
- July 24, 2026