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. 2,565 recalls have been distributed to Kansas in the last 12 months.
Showing 12581–12600 of 28,538 recalls
Recalled Item: Fast-Cath Trio HEMOSTASIS INTRODUCER Recalled by Abbott Medical Due to...
The Issue: Fast-Cath Trio Hemostasis Introducer devices contained 12F sized dilators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fast-Cath Hemostasis Introducer Recalled by Abbott Medical Due to Three lots...
The Issue: Three lots of Fast-Cath Hemostasis Introducer devices contained 8F sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz SE & Co. KG Recalled by Karl Storz Endoscopy Due to The firm has...
The Issue: The firm has become aware that there is a potential that the glass cover at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker T2 Alpha Delta Strike Plate IMN Instruments - part Recalled by...
The Issue: Instrument can break at the level of the thread when being exposed to high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer Recalled by GE...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunar iDXA bone densitometer Recalled by GE Healthcare, LLC Due to An issue...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PuraSinus Absorbable Nasal Hemostat Recalled by 3-D Matrix, Inc. Due to The...
The Issue: The boxes used by the shipper were not validated for use during transport.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPince Full Core Biopsy Instrument 16ga x 15cm. Recalled by Argon Medical...
The Issue: Incorrect product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CardioChek Starter Kit Recalled by Polymer Technology Systems,...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate 3 Mobile Power Unit Recalled by Thoratec Corp. Due to Excessive...
The Issue: Excessive static electricity can potentially cause unrecoverable power loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-se Fiber Optic Miller 2 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickDraw Venous Cannula Recalled by Edwards Lifesciences, LLC Due to If the...
The Issue: If the venous cannula is used in an unintended manner (longer than 6 hours;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Mac 3 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.