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. 2,592 recalls have been distributed to Kansas in the last 12 months.
Showing 10441–10460 of 28,538 recalls
Recalled Item: A.L.P.S. Clavicle Plating System Recalled by Biomet, Inc. Due to The...
The Issue: The instruments may become cold welded together when the drill is inserted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The EOSedge system may acquire two simultaneous orthogonal planar images...
The Issue: Inadequate images resizing and 2D measurement errors may occur when biplanar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wako HDL-C/LDL-C Calibrator - Product Usage: designed to be used Recalled by...
The Issue: FUJIFILM has become aware that incorrect concentration values were printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott i-STAT CG8+ cartridges - IVD Intended for quantitative measurement...
The Issue: Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott i-STAT EG7+ cartridge-IVD. Intended for the quantitative measurement...
The Issue: Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge CM320 Series Washer Disinfector - Product Usage: A multi Recalled by...
The Issue: The potential that the plastic inlet hose connections may deform or break as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set Recalled by...
The Issue: There were customer reports of separation between the tubing and Male Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No....
The Issue: Medical device non-conformance to electrical safety standard (IEC 60601-1).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Acapella DH Vibratory PEP Device - Product Usage: a Recalled by...
The Issue: Shipping box may contain wrong model.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700...
The Issue: Misleading error messages and a gap in the Operator Manual which affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Multirall 200 overhead lift- overhead lift is a general-purpose...
The Issue: Multirall Q-link strap lock has not been fully engaged in the S65 rail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSABOND AB 40 GRAMS FORMULATION 2 Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential heat and humidity exposure. The affected lot contained an atypical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALung Technologies Hemolung Respiratory Assist System (RAS) with CME...
The Issue: CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laerdal Compact Suction Unit (LCSU 4) Recalled by Laerdal Medical (Suzhou)...
The Issue: Component failures may cause the unit to lose all suction. Users will need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnshLabs - SARS-CoV2 IgM ELISA (u-Capture) Recalled by Ansh Labs, LLC Due to...
The Issue: Labeling update; To reduce the risk of false positive/false negative results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...
The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...
The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Medical Care NaturaLyte Liquid Acid concentrate-Liquid Acid...
The Issue: Bottles Missing Product Label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A calculator/data processing module for clinical use is an electronic...
The Issue: A software error results in the unintentional removal of the serum-indices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXOGEN Ultrasound Coupling Gel Recalled by Bioventus, LLC Due to Product may...
The Issue: Product may contain white particulates that are microbial in nature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.