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. 2,630 recalls have been distributed to Nebraska in the last 12 months.
Showing 5041–5060 of 49,150 recalls
Recalled Item: Amingo. OUS only. Recalled by Datex-Ohmeda, Inc. Due to Potential issue that...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire 7900. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auxiliary Common Gas Outlet (ACGO) conversion/install kits sold under...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aespire View. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ion Endoluminal System Recalled by Intuitive Surgical, Inc. Due to There is...
The Issue: There is a potential that the robotic system's instrument cart arm may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys CS2. This anesthesia gas machine is intended to provide Recalled by...
The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NavaClick Syringe and Needle Recalled by LINEAGE BIOMEDICAL, INC Due to...
The Issue: Incorrect GTIN number on carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gold Hard Steel Plus Liquid Recalled by Supercore Products Group Inc. Due to...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis found products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hard Steel Capsules packaged in 1 count blister packs in boxes of 10...
The Issue: Marketed without an approved NDA/ANDA: FDA analysis found products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Umary Acido Hialuronico Recalled by SoloVital Due to Undeclared Diclofenac
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Al'Fez Natural Tahini in 5.6oz glass jars Recalled by AB WORLD FOODS US INC...
The Issue: Potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Elin Dessert Plates. The recalled plates are lilac in color with orange...
The Issue: Elevated levels of cadmium in plates
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by Endo Pharmaceuticals,...
The Issue: Labeling: Label Error on Declared Strength; Some cartons were incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The VITROS XT Chemistry Products ALB-TP Slides is a single Recalled by...
The Issue: The reason for this recall is QuidelOrtho has determined that during normal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guidewire 70cm x 1mm (0.038 ) These accessories Recalled by Bard Peripheral...
The Issue: Due to guidewires being manufactured incorrectly with the guidewires being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...
The Issue: Due to a software issues, after the instrument processes 250 racks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...
The Issue: Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora 3 Series Recalled by DKK Dai-Ichi Shomei Co., Ltd. Due to The weld on...
The Issue: The weld on the light head frame can crack which could lead to problems such...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BKIT BD Pyxis QFill Replenishment Station Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis QFill Replenishment Station Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.