The Anspach Effort, Inc.: Medical Device Recall in 2016 - (Recall #: Z-2253-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of the cranium and spine.

Product Classification:

Class II

Date Initiated: June 15, 2016

Date Posted: July 27, 2016

Recall Number: Z-2253-2016

Event ID: 74447

Reason for Recall:

The graphics at the attachment interface indicating locked and unlocked position are reversed.

Status: Terminated

Product Quantity: 18

Code Information:

Lot #'s: H29309439804, H44310033104, K09311396703, and K09311396704.

Distribution Pattern:

Worldwide Distribution: US Distribution to states of: GA and FL; and country of: Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated