Northgate Technologies, Inc.: Medical Device Recall in 2021 - (Recall #: Z-1147-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device will maintain an expanded cavity (pneumoperitoneum) to allow the insertion of a variety of surgical instruments through the abdominal wall for visual examination of the interior or for surgery (laparoscopic surgery).

Product Classification:

Class II

Date Initiated: January 15, 2021

Date Posted: March 3, 2021

Recall Number: Z-1147-2021

Event ID: 87231

Reason for Recall:

An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.

Status: Terminated

Product Quantity: 25 units

Code Information:

Lot Codes: 9855JEG to 93879JEG

Distribution Pattern:

US Nationwide distribution in the states of FL and OH.

Voluntary or Mandated:

Voluntary: Firm initiated