Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NCB Proximal Lateral Tibia Recalled by Zimmer Biomet, Inc. Due to Non-highly polished implants may adhere to the LDPE...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Biomet, Inc. directly.
Affected Products
NCB Proximal Lateral Tibia, "NCB-PT LAX PROX 3H TIBIA", Various Sizes, Item Nos. 0202261205 0202261207 0202261209 0202261213 0202261305 0202261307 0202261309 0202261313
Quantity: 5,459,583 total devices
Why Was This Recalled?
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Biomet, Inc.
Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report