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. 2,598 recalls have been distributed to Kansas in the last 12 months.
Showing 7681–7700 of 28,538 recalls
Recalled Item: VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog Recalled by...
The Issue: OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Early Bird Bleed Monitoring System Introducer Sheath Set Recalled by...
The Issue: Bleed monitoring system device design error, causing the device to not power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane- Model No. 11327600 Artis icono floor- Model No....
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q floor- Model No. 10848280 Artis Q ceiling- Model Recalled by Siemens...
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno- Model No. 10849000 Recalled by Siemens Medical Solutions USA,...
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The BioZorb LP Marker is an implantable radiopaque marker used Recalled by...
The Issue: Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...
The Issue: Firm noted an increase in customer reports of leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...
The Issue: Burns of varying degrees can occur to patients with electrodes left in while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CorVocet Biopsy System/Catalog Code: CORA1610/B Recalled by Merit Medical...
The Issue: Biopsy Systems have components that are misaligned due to an issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CorVocet Biopsy System Recalled by Merit Medical Systems, Inc. Due to Biopsy...
The Issue: Biopsy Systems have components that are misaligned due to an issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...
The Issue: The outer label does not match the device inside the package. The affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...
The Issue: The outer label does not match the device inside the package. The affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER Recalled by MEDLINE...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by MEDLINE...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FABCO ORS DENTAL ROLLS Recalled by Carwild Corporation Due to Sterility with...
The Issue: Sterility with new cotton source not validated
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites Recalled by...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MaxGuard Flow Controller Extension Set with Needleless Y-Site Recalled by...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.