Device recall

Z-0651-2014: The Vantage Digital Panoramic System delivers high-value features standard on…

FDA device recall · Class II · Midmark Corp dba Progeny Inc

Key facts

Recall number (Z-number) Z-0651-2014
Recall event 66603
Product The Vantage Digital Panoramic System delivers high-value features standard on every system: - Five pre-programmed exam settings, including bitewing, minimize exam set-up time and allow routine diagnostic exams to be performed extraorally for improved clinical efficiency and patient experience…
Product code MUH
Recalling firm Midmark Corp dba Progeny Inc
Recall class Class II
Status Terminated
Termination date Dec 27, 2017
510(k) numbers K122643
FEI number 3000210017

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 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

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