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 28861–28880 of 49,150 recalls
Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...
The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...
The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BuPROPion HCL Tablets Recalled by Mckesson Packaging Services Due to Failed...
The Issue: Failed Moisture Limits: Product tested out-of-specification for moisture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methocarbamol Recalled by American Pharmaceutical Ingredients LLC Due to...
The Issue: CGMP Deviations: Lack of quality assurance at the API manufacturer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE Recalled...
The Issue: The firm was notified that the product may contain peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste NET...
The Issue: The firm was notified that the product may contain peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP...
The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G...
The Issue: Product mislabel. Lot 6291768 of the BD Insulin Syringes with the BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LX3 Floor Stand for LuxOR Ophthalmic Microscope Recalled by Alcon Research,...
The Issue: Multiple shipments or forceful impact to a caster on a LuxOr/LX3 microscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium iCAST Balloon Expandable Covered Stent Recalled by Atrium Medical...
The Issue: Firm received a complaint that a customer who ordered an ADVANTA V12 7mm x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...
The Issue: Carestream found a single unit where four screws in the assembly were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OrthoPACS software. Recalled by Merge Healthcare, Inc. Due to A...
The Issue: A migrated study that has annotations will display the annotations, but when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung GU60A system- Digital X-ray Imaging Systems are intended for...
The Issue: When performing the Stitching function on GU60A system, unintended area is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OrthoPACS software. The firm name on the label is Merge Healthcare...
The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrohydraulic lithotripter probe Recalled by Northgate Technologies, Inc....
The Issue: The inner and outer labels on the product contain incorrect number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mefenamic Acid Recalled by Shionogi Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mefenamic Acid Capsules Recalled by Shionogi Inc. Due to Presence of foreign...
The Issue: Presence of foreign substance: The recall was initiated due to black...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PONSTEL (Mefanamic Acid) USP Recalled by Shionogi Inc. Due to Failed...
The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magellan Diagnostics LeadCare Ultra and LeadCare Plus test Kits. Product...
The Issue: Underestimates the lead concentration of venous blood samples when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIMADZU RADspeed Pro Catalog Number: RADspeed Pro Recalled by Shimadzu...
The Issue: Cracks may occur over time on the tube holding shaft near the base of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.