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

Recall Z-1680-2021 — NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77364

U.S. FDA — Device Enforcement · United States · 2021-03-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1680-2021
Date of alert
2021-03-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Nobel Biocare Procera LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
173943753
Reported risk: Not manufactured to specification
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.