- Recalling firm
- Stryker Sustainability Solutions
- Reason for recall
- Incomplete seals on sterile product
- Affected products (lot / model / serial)
- UDI 00885825006983, Lot Numbers: 3430230, 4648604, 4945422, 4999751, 5044134, 5059493, 4454505, 4882788, 4950218, 4999755, 5044135, 5086419, 4454517, 4945388, 4993562, 5044132, 5044136, 5086420, 4648603, 4945405, 4993565, 5044133, 5044137.
- Units affected
- 24 units
- Distribution pattern
- US Nationwide and the countries of Israel and Canada.
- Firm location
- Tempe, AZ, United States
- Recall type
- Voluntary: Firm initiated
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2190-2026
- Recall initiated
- April 10, 2026
- FDA classification date
- May 13, 2026
- FDA report date
- May 20, 2026
- FDA event ID
- 98708
- Last updated on HTM Vibe
- July 24, 2026