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. 2,634 recalls have been distributed to Nebraska in the last 12 months.
Showing 3781–3800 of 49,150 recalls
Recalled Item: Ambler Surgical Bipolar Pencil 25 Gauge Straight. Model/Catalog Number:...
The Issue: Potential for the outer stainless-steel tube to break or detach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nidek Co. Disposable Bipolar Pencil 25 Gauge Straight. Model/Catalog Number:...
The Issue: Potential for the outer stainless-steel tube to break or detach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accutome/Microsurgical Disposable Bipolar Pencil 5 in. (12.7cm) 25 Gauge...
The Issue: Potential for the outer stainless-steel tube to break or detach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kirwan Surgical Products LLC Disposable 25-gauge bipolar pencil Recalled by...
The Issue: Potential for the outer stainless-steel tube to break or detach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis CII Safe ES Recalled by CareFusion 303, Inc. Due to Due to a...
The Issue: Due to a software issue, automated dispensing cabinet devices may open the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES 7 Drawer Auxiliary Tower Recalled by CareFusion 303,...
The Issue: Due to a software issue, automated dispensing cabinet devices may open the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Due to a...
The Issue: Due to a software issue, automated dispensing cabinet devices may open the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kissable Diabetics Foot Cream Recalled by Brands International Corporation...
The Issue: CGMP Deviations: lack of adequate release testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: The DxI 9000 Access Immunoassay Analyzer wash wheel mixer may not spin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Recalled...
The Issue: Increase in complaints associated with a molding defect within the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aerin Medical VivAer Stylus Recalled by Aerin Medical, Inc. Due to Some...
The Issue: Some units in a single production lot were programmed incorrectly which will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST REPROCESSED BRUNS CURETTE #00 (BC00) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Flex reagent cartridge Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics is recalling two lots of their Dimension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500) Recalled by MEDLINE INDUSTRIES, LP...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE MAGILL FORCEP (MAGF9) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O.R. SCISSORS Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUMMELL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Weak seals...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE STRT KELLY HEMOSTAT (SK8039S) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST IUD REMOVAL HOOK 10" (504090) Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Weak seals may result in a breach of sterility, which may not be detectable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venofer (iron sucrose) Injection Recalled by American Regent, Inc. Due to...
The Issue: Presence of Particulate Matter: Potential for glass delamination from the vials.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.