Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2778-2020 — Anjon Bremer Molded Crown. bone fixation fastener for spinal use. REF number 100048 - Product Usage: Smooth or threaded metallic bone fixation fastener. Provides cervical spine immobilization and therapeutic traction for treatment of patients with cervical trauma or other neck conditions.

U.S. FDA — Device Enforcement · United States · 2020-06-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2778-2020
Date of alert: 2020-06-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Anjon Holdings
Product category: device
Product type: Devices

Reported risk: High rate of galling of one threaded component.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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