⚠ Recalls found. Brand Name is named in 2 official recalls in our current data:
FDA Class II recall Z-2578-2026 — Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
FDA Class II recall Z-1946-2026 — 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 sterile barrier may lead to clinically insignificant extension of surgery or infection leading to surgical intervention.
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…