Brand Name recall — Zimmer, Inc.
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
Official ID Z-2578-2026 · Official record ↗
7 recent recalls on record for Zimmer in CPSC, NHTSA, and FDA data as of July 24, 2026 at 1:09 AM UTC.
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
Official ID Z-2578-2026 · Official record ↗
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Official ID Z-2531-2026 · Official record ↗
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Official ID Z-2530-2026 · Official record ↗
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Official ID Z-2529-2026 · Official record ↗
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Official ID Z-2528-2026 · Official record ↗
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Official ID Z-2527-2026 · Official record ↗
Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or peeling seals. Compromised…
Official ID Z-1946-2026 · Official record ↗
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Compiled from official public-domain government data. Last checked July 24, 2026 at 1:09 AM UTC.