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

Recall Z-1933-2013 — Indus Invue Screw Caddy, Model: SI70097 The caddy holds, in an organized fashion within the case, a variety of shapes and sizes of plates and screws used during fixation of anterior cervical plates to provide stabilization during the development of spine fusions. There is an array of 108 holes th

U.S. FDA — Device Enforcement · United States · 2013-06-21 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1933-2013
Date of alert: 2013-06-21
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: SpineFrontier, Inc.
Product category: device
Product type: Devices

Reported risk: Difficulty removing screws from the Invue caddies.

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.

Related