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. 2,450 recalls have been distributed to Nebraska in the last 12 months.
Showing 23861–23880 of 49,150 recalls
Recalled Item: Arnica Power Recalled by Sprayology Due to CGMP Deviations: products...
The Issue: CGMP Deviations: products manufactured by contract manufacturer under...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bone Builder Recalled by Sprayology Due to CGMP Deviations: products...
The Issue: CGMP Deviations: products manufactured by contract manufacturer under...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Topical Solution Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Defective Container: Repetitive complaints received indicating pump not working.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Melissa's Hatch Chile Clean Snax Recalled by World Variety Produce Inc. Due...
The Issue: Firm discovered that Hatch Chile Clean Snax lists peanuts in the ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Theragenics Applicator Needle (18g x 20cm) The device is comprised Recalled...
The Issue: Some of the pouches containing Brachytherapy Applicator Needles (18g x 20cm)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg Recalled by...
The Issue: Discolored powder has confirmed the presence of a foreign substance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg Recalled by...
The Issue: Discolored powder has confirmed the presence of a foreign substance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 3K 2.5 Ca 1 Mg Recalled by...
The Issue: Discolored powder has confirmed the presence of a foreign substance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightMatter Guide Recalled by Synaptive Medical Inc Due to This recall has...
The Issue: This recall has been initiated due to a software defect found in the Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentamicin Sulfate Ophthalmic Solution Recalled by Akorn, Inc. Due to...
The Issue: Presence of Particulate Matter: Crystalline particles were noticed at the 24...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility; bags have the potential to leak
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by ICU Medical Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; bags have the potential to leak
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Recalled by...
The Issue: VITROS Chemistry Products dLDL Reagent GENs 26 and 27, negatively biased results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spirit Plus Bed Recalled by Stryker Medical Division of Stryker...
The Issue: The beds with the high rail side rail option may not be complaint with IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spirit Select Bed Recalled by Stryker Medical Division of Stryker...
The Issue: The beds with the high rail side rail option may not be complaint with IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by LUPIN SOMERSET Due to...
The Issue: Failed Impurities/Degradation Specifications:Out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide capsules Recalled by Amerigen Pharmaceuticals Inc. Due to...
The Issue: Failed dissolution specifications: Out-of-Specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Giraffe Omnibed - Product Usage: The OmniBed is a combination Recalled by...
The Issue: GE Healthcare has become aware of a potential safety issue that can occur if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemoglobin A1c Control Recalled by Tosoh Bioscience Inc Due to Tosoh...
The Issue: Tosoh Bioscience has become aware of potential degradation of HbA1c control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HEALTHCARE CARESCAPE R860 Inspiratory Safety Guard Recalled by GE...
The Issue: The ventilator Inspiratory Safety Guard (ISG) may disconnect from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.