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. 2,573 recalls have been distributed to Kansas in the last 12 months.
Showing 11121–11140 of 50,117 recalls
Recalled Item: MEDLINE 24 BLOOD CLUTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANKUR Golden Raisin Recalled by Muktanand Foods Inc Due to Undeclared Sulfites
The Issue: Undeclared sulfites
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR Recalled by...
The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product/Part: MitraClip NTR Clip Delivery System US/CDS0601-NTR Recalled by...
The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product/Part: MitraClip G4 CDS NT REPAIR-MR Clinical/CDS0704-NT Recalled by...
The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter Recalled by...
The Issue: Manufacturing error resulted in potential contamination of Bi-Directional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTURION SnagFree Chest Tube insertion Tray Recalled by MEDLINE INDUSTRIES,...
The Issue: One lot of chest tube insertion trays, containing a silk suture component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima Coil System Model Number OPTI0208CSS10 Recalled by BALT USA, LLC Due...
The Issue: Product pouch label does not match up with carton label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wisp and Wisp Youth Nasal Mask Recalled by Philips Respironics, Inc. Due to...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DreamWisp Nasal Mask with Over the Nose Cushion Recalled by Philips...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics Amara View Minimal Contact Full-Face Mask Recalled by...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Therapy Mask 3100 NC/SP Recalled by Philips Respironics, Inc. Due to No...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics DreamWear Full Face Mask Recalled by Philips...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clip COVID Rapid Antigen Test Kit (25-pack) Recalled by LUMINOSTICS, INC dba...
The Issue: COVID test kit shelf life was periodically extended, as real-time stability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Starling Monitor Recalled by Baxter Healthcare Corporation Due to Labeling...
The Issue: Labeling has incorrect or incomplete Unique Device Identification (UDI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy Hand Sanitizer Recalled by SUPERIOR GLOVE WORKS, LTD. Due to CGMP...
The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Recreo Hair Growth Laser Comb Recalled by OMM Imports, Inc. dba Zero Gravity...
The Issue: The firm distributed the laser products without affixing the warning,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Surgical Level 3 Gown Recalled by Texas Medical Technology Inc....
The Issue: Surgical gowns recalled due to gown fabric failing to pass the hydrostatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride Jelly USP Recalled by Akorn, Inc. Due to cGMP...
The Issue: cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Ophthalmic Ointment USP Recalled by Akorn, Inc. Due to cGMP...
The Issue: cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.