- Recalling firm
- Katalyst Surgical, LLC
- Reason for recall
- Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Affected products (lot / model / serial)
- Lot Code: Model No: DVF4005-25 UDI-DI: (01)10817489021665(11)250924(17)280924(10)M50530 Lot Number: M50530 Expiration Date: 09/24/2028
- Units affected
- 10 units
- Distribution pattern
- Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
- Firm location
- Chesterfield, MO, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2070-2026
- Recall initiated
- March 25, 2026
- FDA classification date
- May 6, 2026
- FDA report date
- May 13, 2026
- FDA event ID
- 98660
- Last updated on HTM Vibe
- July 24, 2026