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. 2,634 recalls have been distributed to Nebraska in the last 12 months.
Showing 3941–3960 of 28,140 recalls
Recalled Item: Replacement Battery List Number SUB0000594 and SUB0000864 found in Plum...
The Issue: Due to a manufacturing defect from the battery supplier, affected batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Laparoscopy Litho Std Pack convenience kit and...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Biopsy Drape Pack convenience kit Recalled by...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Special Procedure Pack convenience kit Recalled by...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Cataract Pack convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Hand Pack convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Extremity convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Spine Pack convenience kit Recalled by American...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Contract Systems Gyn Laparoscopy convenience kit Recalled by...
The Issue: Product released with insufficient aeration time impacting the kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaGuide 2 Intelligent Ultrasound Recalled by NovaSignal Corp. Due to Due...
The Issue: Due to inadvertently disconnecting grounding cable of ultrasound system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaGuide 2 Traditional Ultrasound Recalled by NovaSignal Corp. Due to Due...
The Issue: Due to inadvertently disconnecting grounding cable of ultrasound system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX - Magnetic Resonance (MR) systems are Medical Recalled by...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T TX for PET Model Number (REF): 781479 Recalled by Philips North...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AchievaXR -Magnetic Resonance (MR) systems are Medical Electrical Systems...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T S Model Number (REF): 781347 Recalled by Philips North America...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to Ingenia Elition X - Magnetic Resonance (MR) systems Recalled by...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T- Magnetic Resonance (MR) Recalled by...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade dStream - Magnetic Resonance (MR) systems are Medical Electrical...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion- Magnetic Resonance (MR) systems are Medical...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.