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. 2,349 recalls have been distributed to Nebraska in the last 12 months.
Showing 44461–44480 of 49,150 recalls
Recalled Item: Stryker 1) Asnis III Cannulated Screw 4.0x40mm TL Recalled by Stryker...
The Issue: Stryker received a report that the length of the cannulated screw asnis III,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Suction Wand Model S099B Recalled by Sorin Group USA,...
The Issue: Sorin Group is recalling certain lots of Edwards Lifesciences Suction Wand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mullins Transseptal Adult 7F Recalled by Medtronic Inc. Cardiac...
The Issue: Medtronic identified a specific labeling issue for specific lots of Mullins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiohead Access Point 1.4 GHz Radiohead Access Point Firmware versions:...
The Issue: IntelliVue Smart-hopping 1.4 GHz Access Point may experience unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pCO2 D788 Membranes. Distributed by Radiometer America Recalled by...
The Issue: RADIOMETER has become aware that some D788 pCO2 membranes can cause biased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The patient support may move in an unintended manner if the footswitch cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...
The Issue: Failed Impurites/Degradation Specifications: Test failure of single largest...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Crave Brothers Les Freres cheese sold with labeling as: Les Freres Recalled...
The Issue: Whole Foods Market announces that it is recalling Crave Brothers Les Freres...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DayQuil Sinex DayTime Sinus Relief (acetaminophen 325 mg and phenylephrine...
The Issue: Unit Dose Mispackaging: Product packaging defect which could result in code...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: White plastic bottle with blue cap containing 90 capsules Recalled by NOW...
The Issue: It has been determined that this product contains an undeclared ingredient,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic MiniMed Paradigm Reservoirs Recalled by Medtronic MiniMed Due to...
The Issue: Medtronic is recalling certain lots of Medtronic MiniMed Paradigm Reservoirs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pyridostigmine Bromide Tablets 60 mg Recalled by Core Pharma Llc Due to...
The Issue: Failed Stability Specifications: Pyridostigmine Bromide tablets, is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Somersault Pacific Sea Salt flavor Recalled by Somersault Snack Co., LLC Due...
The Issue: A limited number of packages of 1 ounce Somersault Pacific Sea Salt products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL Recalled by...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER Recalled by Ecolab Inc...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL Recalled by Ecolab...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER Recalled by Ecolab Inc Due...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL Recalled by Ecolab...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER WITH GEL Recalled by...
The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Radiation treatment planning Recalled by Elekta, Inc. Due...
The Issue: Upgrade installation script is designed to overwrite the same pouch files in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.