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 27461–27480 of 49,150 recalls
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by Purdue...
The Issue: Subpotent Drug: The laminate used to make the pouches was reversed such that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MONTERIS MEDICAL NEUROBLATE SYSTEM Recalled by Monteris Medical Corp Due to...
The Issue: The firm received complaints that involved an unanticipated interaction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Network Firewall (Cisco ASA 5506) Recalled by Philips Electronics...
The Issue: Firewall installed with Philips IntelliVue Information Center iX or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to...
The Issue: While reviewing documentation for the next software release of the 2008T, an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK(R) from TELEFLEX Auto Endo5(R) Recalled by Teleflex Medical Due to The...
The Issue: The product has a non-conformity that may cause clips to mislead, jam or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Famotodine has an out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Difco" Agar Noble Recalled by Becton Dickinson & Co. Due to Mislabeling
The Issue: HighPuragar was mislabeled and inadvertently sold as Noble Agar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bisoprolol Fumarate tablets Recalled by Unichem Pharmaceuticals Usa Inc Due...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification for an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SOMATOM Go.Up computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Now computed tomography (CT) x-ray system table Recalled by...
The Issue: The table may become unstable if the nuts on the bolts were not adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosphere System with the following three components: HEM1 Advanced Monitor...
The Issue: Pre-procedural issues related to software defects
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm¿ O2 interventional fluoroscopic x-ray system Recalled by Medtronic...
The Issue: During servicing of certain internal components of the O-Arm O2 Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Birds Eye Baby Sweet Peas Recalled by Pinnacle Food Group, Llc Due to...
The Issue: Product has the potential to be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lorazepam Tablets Recalled by Leading Pharma, LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AIA-900 Automated Immunoassay Analyzer performs three methods of...
The Issue: The firm has become aware of a potential issue that may affect the mixing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magstim Rapid Therapy System consisting of: Rapid Mainframe Recalled by The...
The Issue: Users manuals not supplied with 4800-00T US Rapid Therapy System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.zen model Interventional fluoroscopic x-ray system wireless...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.