Z-2736-2026 Class II Ongoing
FDA device recall Z-2736-2026 was initiated by Medline Industries, LP on June 10, 2026 and is designated Class II. 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… The recall status is ongoing. Affected quantity: 163 kits.
Recall Details
- Product Type
- Devices
- Report Date
- July 22, 2026
- Initiation Date
- June 10, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 163 kits
Product Description
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
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.
Distribution Pattern
US Nationwide distribution in the states of CA and UT.
Code Information
UDI-DI 10198459538827 Kit Lots 26DMB644 26CMC467