Device recall

Z-0043-04: Wire Driver Coupler, Model 7100-045, a component of MicroAire Drill/Reamer Model…

FDA device recall · Class III · Microaire Surgical Instruments

Key facts

Recall number (Z-number) Z-0043-04
Recall event 27301
Product Wire Driver Coupler, Model 7100-045, a component of MicroAire Drill/Reamer Model 7500. Driver couplers are reuseable medical devices, non-sterile, packed one per box and labeled in part ***MicroAire Surgical Instruments, 1641 Edlich Drive, Charlottesville, VA 22911***.
Recalling firm Microaire Surgical Instruments
Recall class Class III
Status Terminated
Termination date Jan 21, 2004
FEI number 2020601

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event

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)