Device recall

Z-0729-03: HCMI operator control panels for chiropractic x-ray systems, Model #HF300…

FDA device recall · Class II · Health Care Manufacturing Inc

Key facts

Recall number (Z-number) Z-0729-03
Recall event 27108
Product HCMI operator control panels for chiropractic x-ray systems, Model #HF300, HF600, HF3SE, and HF3SEE.
Product code KPR
Recalling firm Health Care Manufacturing Inc
Recall class Class II
Status Terminated
Termination date Nov 1, 2004
510(k) numbers K022737
FEI number 1929884

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

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