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. 2,386 recalls have been distributed to Kansas in the last 12 months.
Showing 37621–37640 of 50,117 recalls
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Medley LVP Frame Membrane. Intended use to hold platen Recalled by...
The Issue: Administration of inappropriate quantities of fluid can result, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Medley LVP Bezel Assembly. Intended use to hold platen Recalled by...
The Issue: Administration of inappropriate quantities of fluid can result, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WIZARD2 2-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WIZARD2 5-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apex ARC Hip Stem Recalled by Omnilife Science Inc. Due to Product may...
The Issue: Product may breach the inner and outer sterile pouches during shipping or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill Recalled...
The Issue: Oxford Femoral Drill Guide Lateral IM Adapter may have an undersized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SERFAS 90 degree Energy Probe Recalled by Stryker Endoscopy Due to Stryker...
The Issue: Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol 15 mg Recalled by The Compounding Pharmacy of America Due to Lack...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 1 Recalled by The Compounding Pharmacy of America Due to Lack of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone 20 mg Recalled by The Compounding Pharmacy of America Due to...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 1 Recalled by The Compounding Pharmacy of America Due to Lack of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone 30 mg/ml Solution Recalled by The Compounding Pharmacy of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine 60 mg/ml Solution Recalled by The Compounding Pharmacy of America...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hyaluronic Acid Sodium 28 mg/ml + Lidocaine HCl 3 mg/ml Injection Recalled...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.