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. 1,779 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,779 in last 12 months

Showing 4018140200 of 50,117 recalls

Medical DeviceDecember 19, 2014· Fresenius Kabi USA, LLC

Recalled Item: HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION Recalled by Fresenius Kabi USA, LLC...

The Issue: The lot failed pH specification.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips IntelliVue Information Center iX (release A.00 Recalled by Philips...

The Issue: Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2014· BD Biosciences, Systems & Reagents

Recalled Item: CD8 (Leu-2a) PE (In vitro diagnostic) Recalled by BD Biosciences, Systems &...

The Issue: One lot of CD8 PE is contaminated with CD4 FITC and may cause an unexpected...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2014· BD Biosciences, Systems & Reagents

Recalled Item: Anti-Lambda APC-H7 Recalled by BD Biosciences, Systems & Reagents Due to Two...

The Issue: Two lots of the Anti-Lambda APC-H7 antibody are contaminated with CD38 antibody.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2014· Integra LifeSciences Corporation

Recalled Item: The MAYFIELD¿ Ultra 360 Base Unit for head positioner Recalled by Integra...

The Issue: Through an investigation of complaints, Integra found that there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2014· SpineFrontier, Inc.

Recalled Item: lnline Persuader- PedFuse Pedicle Screw System Recalled by SpineFrontier,...

The Issue: A crack may develop in the handle to the Inline Persuader, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2014· Elekta, Inc.

Recalled Item: Focal Sim radiation therapy treatment planning system Recalled by Elekta,...

The Issue: Incorrect CT to ED when using the Monaco Image Statistics Tool.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2014· Becton Dickinson & Company

Recalled Item: BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula Recalled by...

The Issue: The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the...

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

Class II — Potential Health HazardOngoing
DrugDecember 19, 2014· 3M Company/3m Espe Dental Products

Recalled Item: 3M ESPE Clinpro 5000 (1.1% Sodium Flouride) Recalled by 3M Company/3m Espe...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date - The subject lot is...

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

Class III — Low RiskOngoing
Refund
DrugDecember 19, 2014· Bethel Nutritional Consulting, Inc

Recalled Item: B-Lipo Recalled by Bethel Nutritional Consulting, Inc Due to Marketed...

The Issue: Marketed without an Approved NDA/ANDA; found to contain Lorcaserin, a...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 18, 2014· Reily Foods Co.

Recalled Item: CARROLL SHELBY'S ORIGINAL TEXAS BRAND WHITE CHICKEN CHILI KIT Recalled by...

The Issue: Kits contain peanut and almond allergens that are not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2014· Reily Foods Co.

Recalled Item: CARROLL SHELBY'S ORIGINAL TEXAS BRAND CHILI KIT Recalled by Reily Foods Co....

The Issue: Kits contain peanut and almond allergens that are not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2014· Tai Foong U.S.A., Inc

Recalled Item: The package reads in part "***Northern Chef***GLUTEN FREE Recalled by Tai...

The Issue: Tai Foong USA, Inc. is recalling Northern Chef Lightly Coated Cod Fingers...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 18, 2014· Reily Foods Co.

Recalled Item: WICK FOWLER'S TEXAS STYLE FALSE ALARM Mild Chili Kit Recalled by Reily Foods...

The Issue: Kits contain peanut and almond allergens that are not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2014· Reily Foods Co.

Recalled Item: WICK FOWLER'S FAMOUS TEXAS STYLE 2-ALARM Chili Kit Recalled by Reily Foods...

The Issue: Kits contain peanut and almond allergens that are not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 18, 2014· Sysmex Corporation

Recalled Item: The XN-Series modules (XN-10 Recalled by Sysmex Corporation Due to There is...

The Issue: There is a potential for elevated hemoglobin (Hgb) and impedance platelet...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2014· Spinal Elements, Inc

Recalled Item: Ti-Bond Marketing Literature/Labeling Recalled by Spinal Elements, Inc Due...

The Issue: Spinal Elements is recalling the Ti-Bond related brochures that includes...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2014· Ziemer Usa Inc

Recalled Item: Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform...

The Issue: The devices were not shipped with the Starter Kits.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2014· St Jude Medical Cardiac Rhythm Management Division

Recalled Item: Merlin@home RF Remote Monitoring Transmitter Recalled by St Jude Medical...

The Issue: Transmitter may initiate a software reset resulting in backup operation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes Analyzer Recalled...

The Issue: Chemical component of the F3 Fluid pack and environmental bacterial...

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

Class II — Potential Health HazardOngoing