- Recalling firm
- Stryker Sustainability Solutions
- Reason for recall
- Incomplete seals on sterile product
- Affected products (lot / model / serial)
- UDI 00885825002930, Lot Numbers: 3966097, 4314254, 4490535, 4511367, 4517632, 4607771, 4762688, 4056491, 4401626, 4490540, 4511368, 4567842, 4628229, 4775309, 4137164, 4455383, 4490542, 4511369, 4567844, 4628232, 4875058, 4154024, 4463033, 4490544, 4511370, 4567866, 4628234, 5023284, 4165178, 4472622, 4495807, 4511372, 4567888, 4628242, 5023285, 4250497, 4490533, 4502016, 4511375, 4567898, 4665767, 5069705, 4300586, 4490534, 4511155, 4514004, 4607745, 4762686.
- Units affected
- 61 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-2175-2026
- 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