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. 2,612 recalls have been distributed to Nebraska in the last 12 months.
Showing 8141–8160 of 49,150 recalls
Recalled Item: HUDSON RCI Addipak Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Product dispositioned for scrap for sterility failure investigation that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vegetal Vigra Recalled by APG SEVEN, INC Due to Marketed Without an Approved...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NOVAPLUS GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell...
The Issue: Some surgical glove sterile pouches were not completely sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3T Heater Cooler System Recalled by LivaNova Deutschland GmbH Due to The...
The Issue: The firm's labeling (Quick Guide) contains incorrect information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell Healthcare...
The Issue: Some surgical glove sterile pouches were not completely sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: 4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upper roller bracket (part number 1088370) for the Gen2 gantry Recalled by...
The Issue: It is possible the upper roller bracket in the Radixact System gantry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rasagiline Tablets 0.5mg Recalled by Aurobindo Pharma USA Inc. Due to Failed...
The Issue: Failed dissolution specifications - results obtained were below spec average.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix Pain Relieving Cream (Menthol 7.4%) Recalled by Parker Laboratories,...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix Tri-Active Therapy Cream (Camphor 3.2% Recalled by Parker...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix CBD Therapy Cream (Menthol 7.4%) Recalled by Parker Laboratories, Inc....
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix CBD Clinical Cream (Menthol 7.4%) Recalled by Parker Laboratories,...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%) Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Incisive CT Recalled by Philips Healthcare Due to Philips has identified...
The Issue: Philips has identified three software issues with compliance concerns to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynCardia 50cc TAH-t Recalled by SynCardia Systems LLC Due to Artificial...
The Issue: Artificial hearts contain a epoxy resin that has not been reviewed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS70H Salus Surgical Table Recalled by Skytron, LLC Due to When the control...
The Issue: When the control of the operating table was used in Bluetooth mode, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS70 Salus Surgical Table Recalled by Skytron, LLC Due to When the control...
The Issue: When the control of the operating table was used in Bluetooth mode, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnifuse Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to The...
The Issue: The incorrect product labeling was applied to the product indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting that the device was not charging as expected. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.