Every recall we track for Intersurgical Inc — 12 in all — plus the complaints and injury reports the public filed about them.
Intersurgical recalls blue size 00 Guedel airway devices (ISO 5.0) due to potential occlusion. Affected units include specific lot numbers and serial codes. Consumers should contact for details.
Intersurgical recalls specific light green oropharyngeal airway devices due to potential occlusion. Affected units include certain lot numbers and sizes. Consumers should check their device details and contact Intersurgical for guidance.
Intersurgical recalls size 3 yellow Guedel airways with model 1113090 due to potential small burrs that could be inhaled, causing airway obstruction or infection. Affected units have specific model and lot numbers.
Intersurgical recalls green size 2 Guedel airways with model 1112080 due to potential small burrs that could cause airway blockage, irritation, or infection if inhaled.
Intersurgical recalls i-view video laryngoscope model 8008000 due to potential battery depletion causing faulty operation. Affected units include specific lot numbers and UDI-DI codes.
Intersurgical recalls size 3 laryngeal mask airways with incorrect size 4 markings that may pose health risks. Affected units have model number 8003000 and lot code 32204071.
Intersurgical recalls Smoothbore breathing systems with incorrect 22mm exhalation port (model B0062001) due to gas leakage risk during anesthesia. Affected units include lot numbers 4200283 and 4200286.
Intersurgical recalls specific Superset airway connectors due to potential port cracking in the swivel elbow that could leak. Affected units have lot numbers 2182536-2191591.
Intersurgical recalls specific airway connectors due to potential port cracks that could leak. Affected units have lot numbers 2180448, 2180742, 2181001.
Intersurgical recalls specific airway connectors due to potential port cracks that could leak. Affected models include REF 1898000 with lot numbers 2181793-2191327. Contact for replacement.
Intersurgical recalls specific Superset airway connectors due to potential port cracks that could leak. Affected units include lot numbers 2180531, 2181808, 2182241, 2182533.
Intersurgical recalls flexible breathing circuits with exhalation port 22mm due to risk of blocking during assembly, potentially causing serious patient health issues. Affected units include specific product numbers listed in the recall.
