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. 2,491 recalls have been distributed to Nebraska in the last 12 months.
Showing 18501–18520 of 28,140 recalls
Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Introducer Hausdorf-Lock Atrial Recalled by Cook Inc. Due to...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Radial Access Set Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882478: BrightView X designed for single or dual detector nuclear Recalled...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882482: BrightView XCT 882454 BrightView X upgrade to XCT Recalled by...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882480: BrightView designed for single or dual detector nuclear imaging...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic Recalled by...
The Issue: Certain lots of Sex Hormone Binding Globulin (SHBG) do not meet the thirty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LipiFlow Thermal Pulsation System/LipiFlow Recalled by Tearscience, Inc Due...
The Issue: Labeling: The labeled storage temperature is not consistent with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hidrex USA DP450 Recalled by Hidrex GmbH Due to The device was reclassified...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hidrex USA DVP1000 Recalled by Hidrex GmbH Due to The device was...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daavlin Aquex (DAAV1000) Recalled by Hidrex GmbH Due to The device was...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChemVELOCITY Urine Chemistry System Recalled by Beckman Coulter Inc. Due to...
The Issue: The probe misalignment or bending has the potential to lead to delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage:...
The Issue: Maquet has received several complaints involving the VASOVIEW HEMOPRO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride 14.4 mg...
The Issue: After a receiving a customer complaint for incorrect labeling, BD has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Handset Recalled by COVIDIEN MEDTRONIC Due to...
The Issue: Customer reports of the device handset continuing to operate after release...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 Flex Model #: 393-090 Portable Recalled by Radiometer America Inc Due...
The Issue: Reports that the sample type "cord blood" has been changed into the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ABL800 Model#:All Recalled by Radiometer America Inc Due to Reports that...
The Issue: Reports that the sample type "cord blood" has been changed into the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 7400/7440(MEX) Accelerator Recalled by Siemens Medical Solutions...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The UNI-CP System Recalled by Integra LifeSciences Corp. Due to The firm...
The Issue: The firm received one complaint from one non-US sales representative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON MD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.