Every recall we track for Genicon, Inc. — 18 in all — plus the complaints and injury reports the public filed about them.
Genicon recalls single-use laparoscopic clip appliers (model 360-010-001) due to jamming and clip loading failures. Affected units sold with specific lot codes.
Genicon recalls Aquas PowerFlow Tube Sets due to lack of FDA premarket clearance. These surgical irrigation devices may not be safe for use during laparoscopic procedures.
Genicon recalls its GENILook Model 200-005-251 surgical cannula due to potential plastic tip detachment from metal shaft. Affected units sold with lot number I9613-A.
Genicon recalls Model 210-005-052 universal handles due to potential plastic tip detachment from metal shaft. This could cause injury during use. Affected units sold with lot number I9524-A.
Genicon recalls Model 200-105-152 optical tips due to potential plastic detachment from metal shaft. Affected units sold with lot I7781-C.
Genicon recalls Model 200-105-251 optical tips due to potential plastic detachment from metal shaft. Affected units sold in specific lots.
Genicon recalls Model 200-105-252 optical tips due to potential detachment risk. Check your product for 5mm diameter, 150mm length cannula. No remedy specified in official notice.
Genicon recalls Model 210-005-151 cannulas due to risk of plastic tip detaching from metal shaft. Affected units sold in specific lots; check your product details to determine if recalled.
Genicon recalls Natura Model 210-005-251 cannulas due to potential plastic tip detachment from metal shaft. Affected units sold with lot I8880-A.
Genicon recalls Model 210-005-051 cannulas due to potential plastic tip detachment from metal shaft. This could cause injury during use. Affected units were sold with lot number I8003-A.
Genicon recalls its GENILook Model 200-005-153 universal handle due to potential plastic tip detachment from metal shaft. Affected units have specific dimensions and were sold with certain lot numbers.
Genicon recalls Natura Model 210-105-251 cannulas due to risk of plastic optical tip detaching from metal shaft. Affected units sold in specific lots.
Genicon recalls its GENILook Model 200-005-151 surgical cannula due to potential plastic tip detachment from the metal shaft. Affected units were sold with specific lot numbers and model identifiers.
Genicon recalls Model 200-105-151 optical cannulas due to potential plastic tip detachment from metal shaft. Affected units sold in specific lots.
Genicon recalls Model 210-005-152 surgical cannulas due to potential plastic tip detachment from metal shaft. Affected units sold in specific lots; contact for remedy.
Genicon recalls its GENILook Model 200-005-152 surgical device due to potential plastic tip detachment from metal shaft. Affected units sold with lot number I7717-C.
Genicon recalls disposable specimen retrieval bags that may be used for multiple specimens, risking contamination. Affected units include model 550-000-00:000 with lot I8920 from August 2020.
