Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
FDA device recall Z-2736-2026 · posted 2026-07-15 · Open, Classified
Recall details
- 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.
- Action taken
- On June 10, 2026, the firm began notifying customers via First-Class Mail and email. Customers were instructed to request stickers to over-label the affected convenience kits with a label indicating to remove the affected component and replace it with product from supply. No kits are to be returned.
- Root cause
- Under Investigation by firm
- Status
- Open, Classified
- Product code
- LRO
- Quantity affected
- 163 kits
- Distribution
- US Nationwide distribution in the states of CA and UT.
- Date initiated
- 2026-06-10
- Date posted
- 2026-07-15
- Location
- Northfield, IL
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| Medline General Surgery Tray (K213481) | Medline Industries, Inc. | 2022-05-24 |