- Recalling firm
- Medline Industries, LP
- Reason for recall
- Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health consequences from use of product include clinically insignificant extension of surgery to find another readily available device.
- Affected products (lot / model / serial)
- UDI-DI 10198459538827 Kit Lots 26DMB644 26CMC467
- Units affected
- 163 kits
- Distribution pattern
- US Nationwide distribution in the states of CA and UT.
- Firm location
- Northfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2736-2026
- Recall initiated
- June 10, 2026
- FDA classification date
- July 15, 2026
- FDA report date
- July 22, 2026
- FDA event ID
- 99318
- Last updated on HTM Vibe
- July 28, 2026