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. 2,594 recalls have been distributed to Kansas in the last 12 months.
Showing 9341–9360 of 28,538 recalls
Recalled Item: FLASH Ostial System Recalled by Ostial Corporation Due to Angioplasty system...
The Issue: Angioplasty system has a manufacturing issue that has the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew BHR SQUARE HEADED NAIL Recalled by Smith & Nephew Orthopaedics...
The Issue: The nail head may become detached during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heater Cooler Unit (HCU 30) The device supplies temperature-controlled water...
The Issue: There is the potential for contaminated water to enter parts of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV3 Pipeline Flex Embolization Device with Flex Shield Technology Recalled...
The Issue: Due to potential push wire fractures in the delivery system during use. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pipeline Flex Embolization Device Recalled by Micro Therapeutics Inc, Due to...
The Issue: Due to potential push wire fractures in the delivery system during use. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Juniper Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: Due to intermittent failures of the power supply in the ultrasound system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gore Molding & Occlusion Balloon Catheter Recalled by W. L. Gore &...
The Issue: Complaints received concerning Balloon Catheter leakage from the guidewire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity s System . An automated immunoassay analyzer for Recalled by Abbott...
The Issue: A design defect (hardware and software) allows liquid waste pressure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beta-Hydroxybutyrate Reagent A - Enzyme (unlabeled). in vitro diagnostic...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron CX/DX/LX Beta-Hydroxybutyrate . in vitro diagnostic reagent....
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Beta-Hydroxybutyrate . in vitro diagnostic reagent. Recalled...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent. Recalled by...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Beta-Hydroxybutyrate LiquiColor for Synchron CX/LX/DX. in...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COPAN FLOQSwabs Recalled by Copan Italia Due to A sterility assurance level...
The Issue: A sterility assurance level of 10-6 cannot be guaranteed due to intentional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUABEAM Handpiece Recalled by PROCEPT BIOROBOTICS CORPORATION Due to Scope...
The Issue: Scope tube tip may detach from the telescoping tube, which is attached to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRCUL8 LUXE DVT PREVENTION DEVICE Recalled by Ortho8, Inc. Due to CIRCUL8...
The Issue: CIRCUL8 LUXE DVT PREVENTION DEVICE is marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVEXIA LUXE DVT PREVENTION DEVICE Recalled by Ortho8, Inc. Due to EVEXIA...
The Issue: EVEXIA LUXE DVT PREVENTION DEVICE is marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scorpion Portal Vein Access Set - Product Usage: used to Recalled by Argon...
The Issue: As a result of design changes, sheaths have exhibited cracking/breaking at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX Recalled...
The Issue: Due to failure to acquire pre-market clearance for its high resolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zippie Voyage Recalled by Sunrise Medical (US) LLC Due to The seating system...
The Issue: The seating system unexpectedly detached, which resulted in the seating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.