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. 2,439 recalls have been distributed to Nebraska in the last 12 months.
Showing 25121–25140 of 28,140 recalls
Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...
The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-UP) performed...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Recalled...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Mixing Cup Arrays utilized on VITROS 250 Recalled...
The Issue: Ortho Clinical Diagnostics issued a product correction notification for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova StatStrip/StatSensor Hospital Blood Glucose Meter Recalled by Nova...
The Issue: Revised Battery Instructions for Removal and Expiration Date due to battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill (Fluted-Hard Bone) Recalled by Cayenne Medical Inc. Due to A review of...
The Issue: A review of complaints identified a trend for drills breaking.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariAx Compression Plating System Recalled by Stryker Howmedica Osteonics...
The Issue: Stryker received two reports indicating that during screw insertion under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral...
The Issue: A labeling inconsistency was discovered in which the lidstock states that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Recalled...
The Issue: There is an issue with the Manual Film Composer feature on some CT products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CA 125 II Calibrators For use in the calibration Recalled by...
The Issue: Ortho Clinical Diagnostics issued a Product Correction Notification for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Transradial Artery Access products Arrow Transradial Artery Access...
The Issue: There is a risk that the introducer needles packaged within the kits can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes TomoFix Plates The Synthes J5606-C TomoFix Osteotomy System is...
The Issue: A labeling correction was initiated related to the Surgical Technique Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinica Anterior Lumbar Plate (ALP) system Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Spine, Inc. is initiating a correction regarding the Trinica ALP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Implant Holder for Synfix (TM)-LR the Synthes Implant Holder...
The Issue: Complaints were received which described the SynFix LR implant holder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Track System with enGen Select v5.0 with autoverification enabled...
The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Track System with enGen Custom v3.2.2 (& below) Product The VITROS 5...
The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....
The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Resolute Integrity Zotarolimus-eluting Coronary Stent: Stent ID 3.0 mm...
The Issue: A small number of units in lot number 0006573585 of the Resolute Integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms)...
The Issue: Mindray has identified an issue with V Series Monitor where the V Dock power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.