Every recall we track for Northgate Technologies, Inc. — 7 in all — plus the complaints and injury reports the public filed about them.
Northgate Technologies recalls AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe due to incorrect labeling. This affects specific model numbers and lot codes.
Recall of Northgate Technologies' Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter with Russian, Romanian, Slovak, and Czech language settings misconfigured for high/low power.
Northgate Technologies recalls ConMed 50L abdominal insufflators with incorrect tubing material that could cause failure during surgery. Affected units have lot codes 9855JEG to 93879JEG.
Steris recalls CO2MPACT Endoscopic Insufflator systems with specific lot codes due to incorrect tubing material not tested for use. Affected units may pose risks during medical procedures.
Northgate Technologies recalls ACMI 9FR probes (NTI Catalog 72-00198-0) due to failed biocompatibility testing. This may pose health risks during medical procedures.
Northgate Technologies recalls their AUTOLITH URO-TCH 9FR 54cm probe (NTI Catalog 9-203-0543) due to failed biocompatibility testing. This could pose health risks during medical use.
Northgate Technologies recalls Probe (NTI Catalog 9-900-54) due to failed biocompatibility testing. Affected units may pose health risks from improper material use in medical procedures.
