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. 2,440 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,440 in last 12 months

Showing 2314123160 of 50,117 recalls

DrugFebruary 19, 2019· American Health Packaging

Recalled Item: Lovastatin Tablets USP Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Finished product made with lovastatin drug substance that...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 18, 2019· Avitus Orthopaedics, Inc.

Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to Recalled by Avitus...

The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2019· Avitus Orthopaedics, Inc.

Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to Recalled by Avitus...

The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.

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

Class II — Potential Health HazardOngoing
FoodFebruary 16, 2019· Concord Foods, LLC

Recalled Item: Concord Fresh Success Mild Salsa Seasoning Mix Recalled by Concord Foods,...

The Issue: Product contains undeclared allergen, milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Chocolate Choco Chimps Organic cereal. Net Wt....

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Gorilla Munch Corn Puffs cereal. Net Wt. 10 oz (284 g)...

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Cinnamon Jungle Munch cereal. Net Wt. 10 oz (284 g)...

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2019· Ameditech Inc

Recalled Item: QuickTox 5 Panel Drug Screen DipCard Recalled by Ameditech Inc Due to Mixed...

The Issue: Mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11,...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 15, 2019· Covidien, PLC

Recalled Item: Covidien Force TriVerse electrosurgical device 10 cord-Intended as...

The Issue: Potential for the sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2019· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Analyzer Recalled by Alere San Diego, Inc. Due to The...

The Issue: The polarity of the output of power supply was reversed. Due to polarity of...

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

Class II — Potential Health HazardOngoing
DrugFebruary 15, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Etomidate Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Subpotent Drug.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Bard Peripheral Vascular Inc

Recalled Item: PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane...

The Issue: Complaints received that products packaged with the incorrect introducer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS with Option syngo DE Scan for Single Recalled by...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2019· Bioventus, LLC

Recalled Item: BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device...

The Issue: The firm became aware of the potential for the products' sterile pouch to be...

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

Class II — Potential Health HazardOngoing
DrugFebruary 13, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Lovastatin Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Finished product made with lovastatin drug substance that...

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

Class III — Low RiskOngoing
Refund