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. 2,400 recalls have been distributed to Nebraska in the last 12 months.
Showing 36001–36020 of 49,150 recalls
Recalled Item: Kermit's P4 Hot Sauce Recalled by Kermit, Inc. Due to Undeclared Soy
The Issue: Undeclared soy on product label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kermit's Chipotle Key Lime Barbecue Sauce Recalled by Kermit, Inc. Due to...
The Issue: Undeclared soy on product label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kermit's Medium Mannered Key Lime Barbecue Sauce Recalled by Kermit, Inc....
The Issue: Undeclared soy on product label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ingenuity Flex Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turon Shoulder Impaction Fixture The Turon and RSP Recalled by Encore...
The Issue: During the Turon assembly, the impaction forces caused the polymer, black...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P/N: 9734856 Recalled by Medtronic Navigation, Inc. Due to Specific use...
The Issue: Specific use conditions can increase the possibility of a screwdriver tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reverse Shoulder Prosthesis Stem Impaction Fixture The Turon Recalled by...
The Issue: During the assembly, the impaction forces caused the polymer, black acetal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT-A-CATH Plastic Hub Needles Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: The label on the lid stock of the individual needle packages for a portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P/N: 9735023 Recalled by Medtronic Navigation, Inc. Due to Specific use...
The Issue: Specific use conditions can increase the possibility of a screwdriver tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16-Slice (Air) Computed Tomography X-ray systems. Intended to...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore (Oncology & Radiology) Computed Tomography X-ray...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MILEX PESSARY KIT Recalled by CooperSurgical, Inc. Due to The products have...
The Issue: The products have been identified to have incorrect size prints on the MILEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONSULT(TM) diagnostics hCG CONTROLS Kit Recalled by Biochemical Diagnostics...
The Issue: CONSULT diagnostics hCG Controls have discrepant storage temperatures listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedroxyPROGESTERone/Lidocaine (150 mg/mL/1%) 10 mL Multi-Dose Vial Recalled...
The Issue: Lack of Assurance of Sterility; The firm is recalling all sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betamethasone SP PF (12 mg/mL) Recalled by US Compounding Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility; The firm is recalling all sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine PF (1 mg/10 mL) Recalled by US Compounding Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility; The firm is recalling all sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lincomycin/Lidocaine (300 mg/1%/mL) Recalled by US Compounding Inc Due to...
The Issue: Lack of Assurance of Sterility; The firm is recalling all sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.