Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,423 recalls have been distributed to Kansas in the last 12 months.
Showing 30221–30240 of 50,117 recalls
Recalled Item: MAGNESIUM SO4 10ML MDV 50% INJ Recalled by Key Pharmacy and Compounding...
The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ATROPINE SULFATE 0.5% OPHTH Recalled by Key Pharmacy and Compounding Center...
The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...
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: 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: 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 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: 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: BIGnHARD 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: 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: Nonabsorbable suture anchor system intended to reattach soft tissue to...
The Issue: Manufactured with the incorrect anchor outer body
Recommended Action: Stop using. Contact the manufacturer or your 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: 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: 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: 9310HD Digital Video Capture Modules Product Usage: The 9310HD is Recalled...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.