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. 2,624 recalls have been distributed to Nebraska in the last 12 months.
Showing 5421–5440 of 28,140 recalls
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore with software version V4.8.0.10421 Model:728244 CT...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Big Bore RT with software version V4.8.0.10421- Model: 728242 CT Recalled by...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT on Rails Recalled by Philips North America Due to When preparing...
The Issue: When preparing for CCT Fluoroscopy mode and activating the CCT foot pedal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology with software version V4.8.0.10421...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Affiniti 70 Recalled by Philips Ultrasound, Inc. Due to Their is the...
The Issue: Their is the potential that diagnostic ultrasound systems operating with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200)...
The Issue: Their is the potential that diagnostic ultrasound systems operating with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED-810A Zemits NDPrime Laser products Recalled by Advance-Esthetic LLC Due...
The Issue: Advance-Esthetic LLC failed to comply with the applicable standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...
The Issue: Users of the patient positioning system ORION System can be faced with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...
The Issue: Users of the patient positioning system ORION System can be faced with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDFLEX Recalled by CareFusion 303, Inc. Due to If "Clear All" selected...
The Issue: If "Clear All" selected medications is selected on patient profile, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Encore Medical, LP Due to Mislabeling
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reverse Shoulder System e+ Recalled by Encore Medical, LP Due to Mislabeling
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CereLink ICP Extension Cable (Extension Cable) Recalled by Integra...
The Issue: Firm is expanding the existing recall RES 90457 for the Cerelink, initiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.