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. 2,423 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,423 in last 12 months

Showing 2662126640 of 50,117 recalls

DrugMarch 5, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: Decitabine for Injection Recalled by InvaGen Pharmaceuticals, Inc. Due to...

The Issue: Failed impurities/degradation specifications: Failure to water content and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 5, 2018· Johnson Matthey Inc.

Recalled Item: Morphine Sulfate USP Milled Recalled by Johnson Matthey Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Bioburden out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· Sagent Pharmaceuticals Inc

Recalled Item: methylPREDNISolone Sodium Succinate for Injection Recalled by Sagent...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2018· Novel Laboratories, Inc.

Recalled Item: Lupin Hydrocodone Bitartrate and Homatropine Methylbromide Tablets Recalled...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK hsE2 Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Synthes (USA) Products LLC

Recalled Item: Part no. 690.375 Recalled by Synthes (USA) Products LLC Due to Affected...

The Issue: Affected screw gauges incorrectly measure screws 5.41mm shorter than the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Synthes (USA) Products LLC

Recalled Item: Part no. 690.379 Recalled by Synthes (USA) Products LLC Due to Affected...

The Issue: Affected screw gauges incorrectly measure screws 5.41mm shorter than the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh ST AIA-PACK HbA1c Pretreatment Solution Recalled by Tosoh Bioscience...

The Issue: The assay can potentially generate erroneously elevated or erroneously...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: Tosoh ST AIA-PACK HbA1c Control Recalled by Tosoh Bioscience Inc Due to The...

The Issue: The assay can potentially generate erroneously elevated or erroneously...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Testosterone Recalled by Tosoh Bioscience Inc Due to Asfotase...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Cort Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Prolactin Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK FSH Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Synthes (USA) Products LLC

Recalled Item: Part no. 690.380 Recalled by Synthes (USA) Products LLC Due to Affected...

The Issue: Affected screw gauges incorrectly measure screws 5.41mm shorter than the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK CA 19-9 Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK Fer Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK ¿HCG Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK IGE II Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing