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. 2,347 recalls have been distributed to Nebraska in the last 12 months.
Showing 48761–48780 of 49,150 recalls
Recalled Item: VerifyNow P2Y12 Assay Recalled by Accumetrics Inc Due to The recall was...
The Issue: The recall was initiated by Accumetrics because of a field correction to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow System Recalled by Accumetrics Inc Due to The recall was initiated...
The Issue: The recall was initiated by Accumetrics because of a field correction to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump System Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Hyperbaric Infusion Pump Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass...
The Issue: Ortho sensor in Sunrise, FL is recalling the Graphics User Interface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyro-Tab 0.050mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COBAS AmpliPrep Sample Tube Input Barcode Clips Recalled by Roche Molecular...
The Issue: Certain lots of COBAS AmpliPrep (CAP) S-tube Input (Box of 12 bags 12x24...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMAGE Immunochemistry Systems Rheumatoid Factor (RF) Reagent Recalled by...
The Issue: The recall was initiated because Beckman Coulter has confirmed customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH...
The Issue: Stryker has become aware that there exists a potential for breach of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 30mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 40mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 20mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 40mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 20mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.