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. 2,608 recalls have been distributed to Nebraska in the last 12 months.
Showing 10021–10040 of 49,150 recalls
Recalled Item: BD Ultra-Fine II Insulin Syringe 0.5mL Recalled by Becton Dickinson &...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 170MM - Recalled by...
The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plato 17 Microcatheter: Straight Tip Recalled by Scientia Vascular, Inc. Due...
The Issue: Microcatheters for embolic coil and diagnostic agent introduction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Micro-Fine IV Needle 1 ml Recalled by Becton...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - Recalled by BioFire...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1)...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml Recalled by...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - Recalled by BioFire...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Recalled...
The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREAT NOBIL GRIP Recalled by Preat Corp Due to Product is labeled with an...
The Issue: Product is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartsine Samaritan PAD: SAM 350P semi-automatic defibrillator Recalled by...
The Issue: Automated external defibrillators were potentially distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOPHEN Protein C 5 kit is for in vitro quantitative Recalled by Aniara...
The Issue: New warnings and precautionary statements on product labelling: Reagent 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution Recalled by...
The Issue: MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posaconazole Delayed-Release Tablets Recalled by BIOCON PHARMA INC Due to...
The Issue: Failed Impurities/Degradation Specifications: High Out Of Specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection packaged Recalled...
The Issue: Coffee pods may contain undeclared peanut residue
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve Recalled...
The Issue: Coffee pods may contain undeclared peanut residue
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single Recalled by TWO...
The Issue: Coffee pods may contain undeclared peanut residue
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops...
The Issue: Non-Sterility: FDA analysis found unopened products to have bacterial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.