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. 2,435 recalls have been distributed to Kansas in the last 12 months.
Showing 25801–25820 of 50,117 recalls
Recalled Item: PHENYLephrine 40 mg (PHENYLephrine HCL (USP) 40 mg Recalled by Avella of...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 30 mg Recalled by Avella of...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine 50mg Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate Recalled by Avella of Deer Valley, Inc. Store 38 Due to...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL (10 mcg per mL) in 0.95 Sodium Chloride Recalled by Avella of Deer...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.2% ROPivacaine Recalled by Avella of Deer Valley, Inc. Store 38 Due to...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate Recalled by Avella of Deer Valley, Inc. Store 38 Due to...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ceFAZolin 2 gm in NS 100mL. ceFAZolin Sodium (USP) 2gm Recalled by Avella of...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2" Recalled by Teleflex...
The Issue: The incorrect plastic was used to manufacture the handles of these shears,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive...
The Issue: Incorrect use-by date on the device registration/patient file labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to In 2018, Philips...
The Issue: In 2018, Philips Respironics added foam replacement to the preventive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by BioDiagnostic...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MyLab Seven Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Alpha Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Gamma Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centron Product Usage: Vascular Recalled by Philips Healthcare Due to The...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ Product Usage: Vascular Recalled by Philips Healthcare Due to The first...
The Issue: The first time an operator selects a new procedure type during a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.