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. 2,465 recalls have been distributed to Kansas in the last 12 months.
Showing 20501–20520 of 50,117 recalls
Recalled Item: Phenylephrine Hydrochloride Ophthalmic Solution Recalled by Akorn, Inc. Due...
The Issue: Lack of Assurance of Sterility: Out of specification results for container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish Roe) Recalled by...
The Issue: Potential to be contaminated with Clostridium botulinum.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roland Brand Red Caviar - Whole Grain Lumpfish (Lumpfish Roe) Recalled by...
The Issue: Potential to be contaminated with Clostridium botulinum.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dextroamphetamine Sacharate Recalled by Aurobindo Pharma USA Inc. Due to...
The Issue: Superpotent Drug: Amphetamine Mixed Salts 20mg have been found to be out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium/ Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium /Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ra Medical Systems DABRA Catheter 5F (1.5mm) Recalled by Ra Medical Systems,...
The Issue: The firm has become aware there is a potential problem with its DABRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MotoBand CP Recalled by CrossRoads Extremity Systems, LLC Due to Potentially...
The Issue: Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TherMax Blood Warmer Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: TherMax Blood Warmers may not be in compliance with an electrical safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...
The Issue: The sterile barrier of some devices may have been affected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cautery Tip Cleaner Product Usage: electrosurgical accessory Recalled by...
The Issue: The sterile barrier of some devices may have been affected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...
The Issue: The sterile barrier of some devices may have been affected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Povidone Iodine Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.