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. 2,450 recalls have been distributed to Nebraska in the last 12 months.
Showing 23601–23620 of 49,150 recalls
Recalled Item: SHEER DesenZ Desensitizing Treatment Recalled by CAO Group, Inc. Due to cGMP...
The Issue: cGMP violations noted during the firm's most recent inspection.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fas.TRACT Coagulative Hemostatic Gel Recalled by CAO Group, Inc. Due to cGMP...
The Issue: cGMP violations noted during the firm's most recent inspection.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BeeGentle Honey Flavored Topical Anesthetic Recalled by CAO Group, Inc. Due...
The Issue: cGMP violations noted during the firm's most recent inspection.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Jay Robb Unflavored Egg White Protein Recalled by Agropur MSI Ingredients...
The Issue: JayRobb Unflavored Egg White Protein Product is being recalled due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4Patriots Chicken a la King CONTAINS: Wheat Recalled by 4Patriots, LLC Due...
The Issue: Milk not declared on product label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SODIUM CHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SODIUM CHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Covidien Emprint Standard Percutaneous Antenna with Thermosphere Technology...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revanesse Versa Recalled by Prollenium Medical Technologies Inc. Due to...
The Issue: Labeling error. The product is labeled with an 18 month expiration date,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Short Percutaneous Antenna with Thermosphere Technology...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various GE Magnetic Resonance System on-site software version Product Usage:...
The Issue: Possible incorrect software version loaded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Long Percutaneous Antenna with Thermosphere Technology...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Staclot LA 20 () The Staclot¿ LA and Staclot¿ Recalled by Diagnostica Stago,...
The Issue: There have been reports of shortened (T1-T2) results, where some instances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow CVC 2 Lumen Recalled by Arrow International Inc Due to The lidstock...
The Issue: The lidstock states the incorrect priming volume and flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Staclot¿ LA () The Staclot¿ LA and Staclot¿ LA Recalled by Diagnostica...
The Issue: There have been reports of shortened (T1-T2) results, where some instances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quetiapine Tablets USP 400 mg Recalled by Ascend Laboratories LLC Due to...
The Issue: Presence of Foreign Substance; metal shard found in tablet
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Raindrop Near Vision Inlay Recalled by RVO 2.0, INC Due to During a post...
The Issue: During a post approval study the firm found there was an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Systems Software Version 9.01 Update Kit. Recalled by bioMerieux,...
The Issue: The VITEK¿ 2 Systems Software Version 9.01 software may display incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDS Light Suspension Recalled by Stryker Communications Due to There is a...
The Issue: There is a potential the joint in the suspension of the device is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cap'n Crunch's Peanut Butter Crunch Cereal packaged in 17.1 ounce Recalled...
The Issue: Product tested positive for Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.