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. 2,636 recalls have been distributed to Kansas in the last 12 months.
Showing 2041–2060 of 50,117 recalls
Recalled Item: S7-2t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3-1 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artisan Style 1/2 Loaf Recalled by LEWIS BAKERIES Due to Undeclared Allergen
The Issue: Undeclared allergen: Hazelnut due to mispackaging. Product with hazelnuts...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg Recalled by Lupin...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE HealthCare OEC 9800. Recalled by GE Medical Systems, LLC Due to GE...
The Issue: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HealthCare OEC 9900 Elite C-arm Systems. Recalled by GE Medical Systems,...
The Issue: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sparrow Ascent Patient Controller Recalled by Spark Biomedical Inc Due to...
The Issue: Due to manufacturing issue, neurostimulator device may experience "cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SmartPump Tourniquet Recalled by Stryker Corporation Due to...
The Issue: Tourniquet cuff flange may become detached from the bladder. If leak occurs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT) Recalled by North American Rescue...
The Issue: Device used for unilateral or bilateral occlusion of blood flow to the lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy...
The Issue: Due to two issues: 1. Product contamination (biological foreign matter) that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy...
The Issue: Due to two issues: 1. Product contamination (biological foreign matter) that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy...
The Issue: Due to two issues: 1. Product contamination (biological foreign matter) that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy...
The Issue: Due to two issues: 1. Product contamination (biological foreign matter) that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Budesonide Inhalation Suspension Recalled by Cipla USA, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: A market complaint was received for leakage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeprazole Delayed-release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: Presence of foreign tablets/capsules: presence of foreign Divalproex Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117 Recalled by Philips...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 1.5T Model Numbers (REF): (1) 782116 Recalled by Philips...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 3.0T Quasar Dual Model Number (REF): 781150 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Model Numbers (REF): (1) 781315 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.