Aesculap Implant Systems LLC: Medical Device Recall in 2017 - (Recall #: Z-0947-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Gomco Circumcision Clamps with separate O-Ring Component: The device is packaged non-sterile and has no shelf-life The Gomco clamp is intended to be used for circumcision surgeries

Product Classification:

Class II

Date Initiated: October 28, 2016

Date Posted: January 11, 2017

Recall Number: Z-0947-2017

Event ID: 75937

Reason for Recall:

Aesculap has received complaints of excessive bleeding after use of Gomco Circumcision Clamps.

Status: Terminated

Product Quantity: 437 units

Code Information:

Material Code MG096R (1.1 CM) MG097R (1.3 CM) MG227 (1.45CM) MG228 (1.6CM) MG229 (2.1 CM) MG230 (2.6CM)

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated