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. 2,479 recalls have been distributed to Nebraska in the last 12 months.
Showing 19921–19940 of 28,140 recalls
Recalled Item: Dome Centric component ( 01.04227.005) from the Anatomical Shoulder (AS)...
The Issue: In some cases it has been difficult or not possible to disassemble the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard with Compressor ventilator- Recalled by Carefusion 211 Inc dba...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCA Board Recalled by Carefusion 211 Inc dba Carefusion Due to CareFusion...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Delivery Engine (GDE)- Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexichamber Anti-Static Valved Collapsible Holding Chamber Recalled by FSC...
The Issue: Product had torn/loose seal around the mouthpiece.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5195GM Recalled by Lifeline First Aid LLC Due to Cadillac First Aid Kit is...
The Issue: Cadillac First Aid Kit is recalled because it contains the CPR Shield with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Item # 4042-CPR Rescue Kit Recalled by Lifeline First Aid LLC Due to First...
The Issue: First aid kits or rescue kits are recalled because they contains the CPR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics...
The Issue: If the user selects the Comment or Interpretation option (in the enGEN .gsb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COSEAL Surgical Sealant Kit Recalled by Baxter Healthcare Corp Due to...
The Issue: Potential for incomplete dissolution of the polyethylene glycol (PEG)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19...
The Issue: A patient weight can be populated incorrectly under certain conditions when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 3 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or...
The Issue: Premature bucket failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 10 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 5 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piccolo Composite Tibia and Femoral Nailing Systems - Ball Tip Recalled by...
The Issue: Firm received complaints where the Piccolo Composite Ball Tip Guide Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse PACS software version 4.4.000 Recalled by Fujifilm Medical...
The Issue: Synapse cannot display image files, DICOM SR files, and/or Annotation files....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...
The Issue: The device was found to have bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software error in previous software versions in which two for the same image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.