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. 2,404 recalls have been distributed to Kansas in the last 12 months.
Showing 34881–34900 of 50,117 recalls
Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is Recalled by Arrow...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid Recalled by...
The Issue: Labeling: Label Mix-Up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TEARS Naturale FREE (dextran 70 and hypromellose 2910) lubricant eye drops...
The Issue: Lack of Assurance of Sterility: Some single-use vials may be filled with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Denali Filter-Femoral Delivery System Product Code: DL900F/DL950F Recalled...
The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J...
The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...
The Issue: A report can be confirmed with the incorrect patient demographics resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TF Adaptive Gutta Percha Point Size SM3 50pk Recalled by Ormco/Sybronendo...
The Issue: Ormco Corporation is recalling the TF Adaptive Gutta Percha Point Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire PAL-R4011XL - 40cm x 4 mm Del Vecchio French Rasp aspiration...
The Issue: Complaints that the cannula bent/broke during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device Recalled by...
The Issue: MicroAire has initiated a recall on product PAL-R4011XL (40cm x 4mm Del...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicated Better Braids Recalled by Keystone Laboratories Inc Due to...
The Issue: Microbial Contamination of a Non-Sterile Products: The product had a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tudorza Pressair (aclindinium bromide inhalation powder) Recalled by...
The Issue: Defective Delivery System: Some units have actuation counters set to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paricalcitol Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...
The Issue: PRESENCE OF PARTICULATE MATTER: Product complaint for the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray Systems Recalled by Philips Medical...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano R100 Sterile Equipment Cover Recalled by Volcano Corporation Due to...
The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray Systems Recalled by Philips...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Computed Tomography X-ray Systems Recalled by Philips...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.