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. 927 recalls have been distributed to Kansas in the last 12 months.
Showing 47441–47460 of 50,117 recalls
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GMC51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH S2 Product Code: GSM61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH ST Product Code: GST61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH ST Product Code: GST60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Dens Instrument Set (Dens Graphic Case) Recalled by Synthes USA HQ,...
The Issue: The Dens Instrument Set has been designed to facilitate the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 7 x 24 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 16 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 12 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 8.5 x 24 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 10 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 5 x 24 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 14 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation...
The Issue: Does Not Meet Monograph: Budesonide may be slightly above or below the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30...
The Issue: Does Not Meet Monograph: Budesonide may be slightly above or below the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spice Cake Mix Recalled by Jiffy Food Service, LLC Due to Undeclared Allergen
The Issue: Undeclared Allergen (Milk). Firm initiated a voluntary recall of their 25...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Homestead Creamery Artisan Cheese Recalled by Homestead Creamery Due to The...
The Issue: The raw milk cheese product may be contaminated with shiga-toxin e-coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Furosemide Injection USP (10 mg/mL) Recalled by Hospira, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: There is the potential for solution to leak...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 (rev A and Recalled...
The Issue: Neonatal beds and incubator display boards may randomly overwrite stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.