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 9721–9740 of 28,538 recalls
Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...
The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrodissection Cannula (Chang) Recalled by Anodyne Surgical Due to The...
The Issue: The product may have a yellowish-brown/greenish-brown residue present at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24...
The Issue: Evaluation of a clinical goal for the voxelwise worst dose distributions may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 21 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 17 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 27 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rubber Dam Clamp Recalled by Dentech Corp. Due to Removing parts for safety...
The Issue: Removing parts for safety reasons due to possible breakage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical Video Duodenoscope - Product Usage: intended to be Recalled...
The Issue: IFU updated: The warning section of the IFU for both the OE-A63 distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centaur Syphilis Assay-SYP Kit Recalled by Siemens Healthcare Diagnostics,...
The Issue: Potential for the ADVIA Centaur Syphilis assay to carryover into other...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELUVIA Drug-Eluting Vascular Stent System - Product Usage: indicated for...
The Issue: One batch of the ELUVIATM Drug Eluting Vascular Stent System incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialysate Concentrate for Hemodialysis-Liquid/Powd - Product Usage: used in...
The Issue: The lot may have experienced an anomaly during the manufacturing process,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta MOSAIC Oncology Information System versions: 2.62 Recalled by Elekta,...
The Issue: Malware attack
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multitom RAX with software version VF10 Recalled by Siemens Medical...
The Issue: Siemens identified two issues, In some cases, it is possible to perform an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Logical cup liner - Product Usage: intended to replace a Recalled by...
The Issue: Product mislabeled, with the incorrect product inside the package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Interlock Suspension System Lanyard Body: An external prosthetic...
The Issue: the firm discovered that, starting on April 1, 2020, a 3/8 dowel pin was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Econocare Plus Waffle Overlay- Intended for use as a medical Recalled by...
The Issue: Product contamination-a trace amount of dried bodily fluids may expose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Case Cardiac Assessment System for Exercise Testing and CardioSoft...
The Issue: If a certain sequence of events occur, the pdf test report that belongs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 3 (GTIN 00840682147378) Recalled by GE Healthcare,...
The Issue: The IGS system can experience a single vertical line defect where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Enterprise Viewer - Product Usage: intended to be Recalled...
The Issue: A software defect was identified where the Image Styles defined by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Impacted lot may...
The Issue: Impacted lot may leak inside the ARIES instrument.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.