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. 2,650 recalls have been distributed to Nebraska in the last 12 months.
Showing 641–660 of 49,150 recalls
Recalled Item: Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pouch Bag. Recalled...
The Issue: Undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz. Recalled by...
The Issue: Undeclared pecan
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Yoyo Gummy Tropical Flavor Recalled by SB FOOD LLC Due to The products...
The Issue: The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Yoyo Gummy Grape Plus Flavor Recalled by SB FOOD LLC Due to The products...
The Issue: The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled by Glenmark...
The Issue: Cross Contamination with Other Products: Testing of reserve samples showed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Emphasizing instructions for LVP duration programming located in the IFU.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yoyo Gummy Assorted Flavor Recalled by SB FOOD LLC Due to The products...
The Issue: The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical...
The Issue: Incorrect Product Formulation
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restore Clinician Programmer Application (CP App) Recalled by Medtronic...
The Issue: Software issue where a Device Reset message displayed on the app was unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product...
The Issue: Wire connected to the electrical box may shift out of its intended position,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product...
The Issue: Wire connected to the electrical box may shift out of its intended position,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardware configuration of the BeneVision Central Monitoring System (CMS)...
The Issue: When the Worstation of the BeneVision DMS has a specific hardware...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand name: AGFA Digital Radiography X- Ray system DR 800 Recalled by AGFA...
The Issue: It is possible to exceed the maximum allowed Air Kerma rate (AKR) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nebivolol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Intelerad InteleShare software Recalled by DICOM Grid, Inc. Due to Software...
The Issue: Software intended to aid in diagnosing conditions, planning treatments,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number:...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...
The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Pressio 2 ICP Monitoring System Recalled by Sophysa Due to Customer...
The Issue: Customer complaints of Pressio monitor rebooting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.