Device recall

Z-1680-2021: NPr FCZImp Crwn ASC CC RP CAD 1-25 s4 - Product Usage: Implant Crown intended to…

FDA device recall · Class II · Nobel Biocare Procera LLC

Key facts

Recall number (Z-number) Z-1680-2021
Recall event 87848
Product NPr FCZImp 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
Product code NHA
Recalling firm Nobel Biocare Procera LLC
Recall class Class II
Status Terminated
Termination date Sep 1, 2021
510(k) numbers K132746
FEI number 3005031178

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)