- Recalling firm
- Stryker Sustainability Solutions
- Reason for recall
- Incomplete seals on sterile product
- Affected products (lot / model / serial)
- UDI 00885825006884, Lot Numbers: 3002664, 4092049, 4580888, 4627994, 4778840, 4860529, 4998452, 4026540, 4098358, 4620256, 4627999, 4813542, 4985859, 4072508, 4498128, 4620257, 4755333, 4860528, 4985861.
- Units affected
- 19 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-2188-2026
- 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