The Anspach Effort, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2077-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

.***ANSPACH***Sterile. REF SHD-4820DS***QTY: 1, 4.8 mm x 2mm Twist Drill with Depth Stop. Use with SHORT-HD Attachment ***RX Only Product Usage: Cutting and shaping bone including bones of the spine and cranium.

Product Classification:

Class II

Date Initiated: September 19, 2011

Date Posted: August 1, 2012

Recall Number: Z-2077-2012

Event ID: 62326

Reason for Recall:

Anspach Effort, Inc. Palm Beach Gardens, FL is recalling their Single Use Sterile Bone Cutting Burrs used with XMax, microMax, microMax Plus, eMax, eMax2 and eMax2 Plus High Speed Drill Systems. It is possible for the cutter to come apart.

Status: Terminated

Product Quantity: 5 each

Code Information:

Lot numbers E203050779 and E383055709.

Distribution Pattern:

US Nationwide Distribution including the states of: Arizona. and California.

Voluntary or Mandated:

Voluntary: Firm initiated