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 26721–26740 of 49,150 recalls
Recalled Item: Limbrel (flavocoxid 250 mg) capsules Recalled by Primus Pharmaceuticals,...
The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Limbrel500 (flavocoxid and citrated zinc bisglycinate) 500 mg/50 mg capsules...
The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets...
The Issue: CGMP deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: O-arm 1000 mobile image-intensified fluoroscopic x-ray system Recalled by...
The Issue: Software update ("SW Update 3.2.1") is being implemented to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity...
The Issue: Potential that one or more image series may be missing from an exam without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Product Usage: Usage: Centricity PACS-IW with...
The Issue: Potential that one or more image series may be missing from an exam without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Select Cycler (SW v.2.8.7) Recalled by Fresenius Medical Care Renal...
The Issue: The recalling firm identified a software issue related to the Patient Line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cefuroxime Recalled by JCB Laboratories LLC Due to Subpotent Drug: The...
The Issue: Subpotent Drug: The product is sub-potent prior to its 90-day beyond use date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panera Plain Cream Cheese Recalled by Panera, LLC Due to Potential Listeria...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Reduced-Fat Wild Blueberry Cream Cheese Recalled by Panera, LLC Due to...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ready-to-Eat Powdered Peanut Butter in 1 lb (16 oz.) plastic jars Recalled...
The Issue: Analytical results for generic non-pathogenic E. coli surpassed firm's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Panera Reduced-Fat Plain Cream Cheese Recalled by Panera, LLC Due to...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Panera Chive&Onion Reduced Fat Cream Cheese Spread Recalled by Panera, LLC...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Panera Reduced-Fat Honey Walnut Cream Cheese Recalled by Panera, LLC Due to...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is Recalled by Biomerieux...
The Issue: Missing desiccant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...
The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...
The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo XT Suture Anchor Recalled by Valeris Medical, LLC Due to The label on...
The Issue: The label on Apollo XT 5.5mm Suture Anchor (part # XTS-5515; lots 2358,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prickly Ash Bark Powder Herbal Supplement Recalled by Mountain Rose Inc Due...
The Issue: Prickly Ash Bark Powder is recalled due to a potential contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oxycodone Hydrochloride Tablets Recalled by Ascent Pharmaceuticals, Inc. Due...
The Issue: Labeling; Label Error Not Elsewhere Classified; label missing controlled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.