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. 2,532 recalls have been distributed to Kansas in the last 12 months.
Showing 14961–14980 of 50,117 recalls
Recalled Item: Norton Arm Kit Recalled by Aspen Surgical Products, Inc. Due to Affected...
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jessie Sterile Arm Suspension Kit Recalled by Aspen Surgical Products, Inc....
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marco Shoulder Stabilization Kit Recalled by Aspen Surgical Products, Inc....
The Issue: Affected products were manufactured with materials found to have a bioburden...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUGMENT Injectable Kit Recalled by BioMimetic Therapeutics, LLC Due to The...
The Issue: The kit contains the wrong vial tray in the package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...
The Issue: Potential for leaks and loosening at the patient catheter connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TheraSphere Administration Set Recalled by Boston Scientific Corporation Due...
The Issue: Potential for leaks and loosening at the patient catheter connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hiland 100% Pure Apple Juice From Concentrate No Sugar Added Recalled by...
The Issue: Elevated levels of inorganic arsenic.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baxter prismaflex Recalled by Baxter Healthcare Corporation Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter PrismaFlex Recalled by Baxter Healthcare Corporation Due to Products...
The Issue: Products labeled as sterile were distributed, but may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD" Mouse IgG2a Isotype Control APC X39 ASR Recalled by Becton, Dickinson...
The Issue: Complaints have been received for performance issues related to high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ Ultrasound Systems Recalled by Philips Ultrasound Inc Due to Ultrasound...
The Issue: Ultrasound system control panel arm swivel lock could fail, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxA 5000 (DxA Automation System Recalled by Beckman Coulter Inc. Due to...
The Issue: There is a potential that sample carriers (w or w/o samples) within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB Recalled by Cordis Corporation...
The Issue: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis SUPER TORQUE MB 5F PIG Recalled by Cordis Corporation Due to Cordis...
The Issue: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis SUPER TORQUE MB 5F PIG Recalled by Cordis Corporation Due to Cordis...
The Issue: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL Recalled by Cordis Corporation...
The Issue: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis SUPER TORQUE MB 5F PIG Recalled by Cordis Corporation Due to Cordis...
The Issue: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIAMONDBACK 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM Recalled by...
The Issue: There is a potential mislabeling of the OAD crown sizes: 1.50mm Sold Crown...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM Recalled by...
The Issue: There is a potential mislabeling of the OAD crown sizes: 1.50mm Sold Crown...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MERITMEDICAL Prelude Short Sheath Introducer Recalled by Merit Medical...
The Issue: There is a potential that a package sheath contains an incorrect dilator.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.