- Recalling firm
- Mentor Texas LP
- Reason for recall
- A single lot of expired syringes were distributed due to a distribution system control failure.
- Affected products (lot / model / serial)
- BD Product Code: 302995 Mentor Product Code: B9604 Sales Unit Box UDI-DI/GTIN code: 30382903029952 Individual Unit UDI-DI/GTIN code: 00382903029952 Lot Number: 8298877
- Units affected
- 1401 syringes
- Distribution pattern
- U.S.: CA, FL, and PA
- Firm location
- Coppell, TX, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2614-2026
- Recall initiated
- April 28, 2026
- FDA classification date
- June 26, 2026
- FDA report date
- July 8, 2026
- FDA event ID
- 98981
- Last updated on HTM Vibe
- July 23, 2026