- Recalling firm
- Stryker Sustainability Solutions
- Reason for recall
- Incomplete seals on sterile product
- Affected products (lot / model / serial)
- UDI 00885825003135, Lot Numbers: 2268964, 2687510, 3173767, 3269330, 3379246, 4398753, 4876242, 2501717, 2878890, 3231930, 3336473, 3394078, 4780878, 4876243, 2533915, 3137651, 3266358, 3361335, 3454810, 4821709.
- Units affected
- 28 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-2176-2026
- 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