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. 2,420 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,420 in last 12 months

Showing 3246132480 of 50,117 recalls

Medical DeviceSeptember 19, 2016· Encore Medical, Lp

Recalled Item: Empowr PS Knee System Box Cut Guide The EMPOWER PS Recalled by Encore...

The Issue: It has been discovered that during Empowr PS Total Knee replacement, while...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Bausch & Lomb Inc Irb

Recalled Item: PeroxiClear Peroxide Solution Recalled by Bausch & Lomb Inc Irb Due to...

The Issue: Product was found to contain excess residual levels of hydrogen peroxide.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Pressure Tourniquet Cuff (PTC) Tourniquet cuffs are single- or...

The Issue: Issue with the process for detection of leaking Pressure Tourniquet Cuffs...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 Smart-hopping...

The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 WMTS Smart-hopping...

The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2016· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 802.11a/b/g Product...

The Issue: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting...

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

Class II — Potential Health HazardOngoing
FoodSeptember 17, 2016· Mccormick

Recalled Item: Club Size McCormick Original Taco Seasoning Mix 24 oz. Recalled by Mccormick...

The Issue: Product was recalled due to undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 16, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Marcaine 0.25% (bupivacaine HCl) injection Recalled by Hospira Inc., A...

The Issue: Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Marcaine 0.5% (bupivacaine HCl) injection Recalled by Hospira Inc., A Pfizer...

The Issue: Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 16, 2016· National Foods Packaging Inc

Recalled Item: National Foods Packaging Low Sodium Chicken Base in 50 lb Recalled by...

The Issue: Product contains a spice which was tested and found to contain elevated...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 16, 2016· National Foods Packaging Inc

Recalled Item: Hillcrest Farms Poultry Gravy Mix in 25lb brown poly-lined bags Recalled by...

The Issue: Product contains a spice which was tested and found to contain elevated...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 16, 2016· National Foods Packaging Inc

Recalled Item: National Foods Packaging Chicken Base in 25 lb white poly-lined paper bags...

The Issue: Product contains a spice which was tested and found to contain elevated...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 16, 2016· GE Healthcare, LLC

Recalled Item: Brivo XR385 Recalled by GE Healthcare, LLC Due to The placing of weight on...

The Issue: The placing of weight on the VRAD detector, of the Brivo XR385 digital...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G Recalled by Becton...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2016· Becton Dickinson & Company

Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G Recalled by...

The Issue: BD identified that several lots did not receive the specified dose of...

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

Class II — Potential Health HazardOngoing