Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,538 recalls have been distributed to Nebraska in the last 12 months.
Showing 16341–16360 of 28,140 recalls
Recalled Item: Doyen-Collin Mouth Gag 120MM/ General Instruments Recalled by Aesculap...
The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strauss Penis Clamp 130MM/General Instruments Recalled by Aesculap Implant...
The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic ADT1018 Flow QC Clear Advantage Tubing Recalled by Transonic...
The Issue: The sterility of the device cannot be assured. There is a potential for an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity TF PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: Following a period of inactivity, the mass storage device may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Impression Plus Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS HI Recalled by Siemens Medical Solutions USA, Inc Due to Control...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Avant-garde Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Expression Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M2 / PRIMUS Mid-Energy Recalled by Siemens Medical Solutions USA,...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Impression Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold...
The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled:...
The Issue: The duodenoscopes are being recalled in order to replace the forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaPET¿ RF Latex Reagent used as a component in the Recalled by Stanbio...
The Issue: All patient serum samples yield a weakly positive test result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold...
The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK¿ PROG III Recalled by Tosoh Bioscience Inc Due to Falsely...
The Issue: Falsely elevated progesterone assay values will occur when using certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK¿ PROG II Recalled by Tosoh Bioscience Inc Due to Falsely...
The Issue: Falsely elevated progesterone assay values will occur when using certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Connect 272 KG Scale used with Maxi Sky 2 Recalled by Arjohuntleigh...
The Issue: The spreader bar can detach from the scale attachment under certain conditions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling Recalled by...
The Issue: The spreader bar can detach from the scale attachment under certain conditions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stanbio AC power adapter for the HemoPoint H2 meter Recalled by Stanbio...
The Issue: The US prong (type A) adapter plate may crack, break, or detach and remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.