- Recalling firm
- BD SWITZERLAND SARL
- Reason for recall
- Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.
- Affected products (lot / model / serial)
- Catalog Number: SAM2461 REF: DYNDTN0555 UDI code: N/A Lot Number: 25X445
- Units affected
- 50 devices
- Distribution pattern
- U.S.: IL O.U.S: N/A
- Firm location
- Eysins, N/A, Switzerland
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- N/A
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2654-2026
- Recall initiated
- June 4, 2026
- FDA classification date
- July 2, 2026
- FDA report date
- July 8, 2026
- FDA event ID
- 99085
- Last updated on HTM Vibe
- July 23, 2026