Aesculap, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0623-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with the HiLAN¿ and microspeed motor systems to hold burrs which cut and shape bone.

Product Classification:

Class II

Date Initiated: December 9, 2013

Date Posted: January 15, 2014

Recall Number: Z-0623-2014

Event ID: 67050

Reason for Recall:

Certain lots of the Aesculap Hi Line XXS handpiece (part # GB790R) were recalled due to a possible failure of the handpiece.

Status: Terminated

Product Quantity: 14

Code Information:

Hi-Line XXS handpiece; Part Number - GB790R , Lot Number 4504385018 4504300008 4504328565 4504685847 4804685865

Distribution Pattern:

Worldwide Distribution - USA including TX, NY, PA, and TN. Internationally to Austria, Switzerland, Germany, Denmark, Spain, Finland, France, Hong Kong, Israel, Italy, Japan, Netherlands, Poland, Russian Federation, and Taiwan.

Voluntary or Mandated:

Voluntary: Firm initiated