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 29901–29920 of 49,150 recalls
Recalled Item: ZRECT for Women Herbal Dietary Supplement Capsules Recalled by Organic...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TORNADO Male Enhancement Herbal Dietary Supplement Capsules Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZRECT Male Enhancement Herbal Dietary Supplement Capsules Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UPROAR All Natural Male Enhancement Herbal Dietary Supplement Capsules...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LabidaMAX Herbal Dietary Supplement Capsules Recalled by Organic Herbal...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RECTALIS Male Enhancement Herbal Dietary Supplement Capsules Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cummor Natural Male Enhancement Recalled by Organic Herbal Supply Due to...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ENHANCEROL Herbal Dietary Supplement Capsules Recalled by Organic Herbal...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xrect Male Enhancement Herbal Dietary Supplement Capsules Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZDaily Daily Testosterone and Llibido Booster Herbal Dietary Supplement...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zinc Oxide Paste 25% Recalled by Fagron, Inc Due to Labeling: Error on...
The Issue: Labeling: Error on Declared Strength: Error is due to an incorrect value in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy Relief Diphenhydramine HCl 25 mg Recalled by P & L Development, LLC...
The Issue: Subpotent: This product is being recalled due to low out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail Recalled by...
The Issue: nail not properly engaging with the targeting jig due to certain undersized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to Cardiovascular Systems,...
The Issue: Cardiovascular Systems, Inc. (CSI). has initiated a recall to remove 1,396...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...
The Issue: Software bug which allows parameters to be changed unintentionally during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA...
The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST OXACILLIN OX 256 US F100 In vitro diagnostic Recalled by BioMerieux SA...
The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.