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. 2,419 recalls have been distributed to Nebraska in the last 12 months.
Showing 33581–33600 of 49,150 recalls
Recalled Item: BIOGRAPH 40 TruePoint w/TrueV Recalled by Siemens Medical Solutions USA Inc....
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT Flow 40-4R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT Flow 20-3R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYS IVK Recalled by Siemens Medical Solutions USA Inc. Due to Siemens...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH 64-3R TruePoint Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph Sys 16-3R to 16-4R upgrade Recalled by Siemens Medical Solutions...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOGRAPH mCT Flow Edge-3R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streamline OCT Occipito-Cervico-Thoracic System Recalled by RTI Surgical,...
The Issue: Potential for a product defect where the cannula may be obstructed. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS pharmacy Original Strength Acid Controller tablets Recalled by Dr....
The Issue: Failed impurities/degradation specification: An out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant...
The Issue: AFT Diverted Tubes are being recalled due to a customer complaint involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitaTops Apple Crumb Recalled by Vitalicious Acquisition Due to Undeclared Milk
The Issue: The affected lots of VitaTops Apple Crumb contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and...
The Issue: Operators noticed unwanted release of evaporating anesthetic agent at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate 25mcg/mL in 0.9% Sodium Chloride 30 mL fill Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine 16 mg added to 0.9% sodium Chloride Recalled by Pharmakon...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 10 Units added to Lactated Ringers in a 500 mL lntravia bag...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.