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. 2,524 recalls have been distributed to Nebraska in the last 12 months.
Showing 17641–17660 of 28,140 recalls
Recalled Item: Tissu-Trans Filtron 250 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to Seal...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans SFILL 360 Recalled by Shippert Medical Technologies Due to Seal...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 100 Recalled by Shippert Medical Technologies Due to...
The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
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: BD Precision Glide Needle 18G x 1 RB Recalled by Becton Dickinson & Company...
The Issue: Hub damage resulting in breakage and/or leakage during use.
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: 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: 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: 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: 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: 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: 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: 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: Magellan Diagnostics LeadCare and LeadCare II test Kits. Product Usage:...
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: 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 Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number:...
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.
Recalled Item: Ultrasound Video Gastroscope Recalled by Pentax of America Inc Due to Error...
The Issue: Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used...
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.