Device recall

Z-1614-2010: 7.5MM Bone Tap, Modular; Manufactured by: Blackstone Medical, Inc. 1720 Bray…

FDA device recall · Class II · Blackstone Medical, Inc.

Key facts

Recall number (Z-number) Z-1614-2010
Recall event 55508
Product 7.5MM Bone Tap, Modular; Manufactured by: Blackstone Medical, Inc. 1720 Bray Central Drive, McKinney, TX 75069. Intended to created a screw thread in a hole drilled into bone to facilitate placement of a bone screw.
Product code HWX
Recalling firm Blackstone Medical, Inc.
Recall class Class II
Status Terminated
Termination date Aug 10, 2010
FEI number 3001238051

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 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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