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. 2,370 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,370 in last 12 months

Showing 4116141180 of 50,117 recalls

DrugOctober 30, 2014· Baxter Healthcare Corp.

Recalled Item: Heparin Sodium in 0.9% Sodium Chloride Injection Recalled by Baxter...

The Issue: Subpotent Drug: Heparin raw material was found to have low potency

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2014· Radiometer America Inc

Recalled Item: Crea A and B membranes Recalled by Radiometer America Inc Due to Negative...

The Issue: Negative drift on QC during in-use lifetime of CREA membranes can be observed.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2014· Respironics California Inc

Recalled Item: Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit...

The Issue: If the power supply fan mounting screws are installed incorrectly, the ends...

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

Class II — Potential Health HazardOngoing
FoodOctober 29, 2014· Mt. Olive Pickle Company Inc

Recalled Item: Mt. Olive Recalled by Mt. Olive Pickle Company Inc Due to Product may...

The Issue: Product may contain glass fragments.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 28, 2014· Marathon Ventures Inc

Recalled Item: Macadamia nuts in various formats: (1.) Western Family Macadamia Diced Nuts...

The Issue: Macadamia nuts may have possible contamination with Salmonella florida.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 28, 2014· Cooper Vision Caribbean Corp.

Recalled Item: Soft Contact Lens Recalled by Cooper Vision Caribbean Corp. Due to Portions...

The Issue: Portions of the lots may contain units with an incorrect lens axis condition.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Inspiration system: Product Usage: mammography exams Recalled by...

The Issue: It was determined that if the Mammomat Inspiration system is not secured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2014· CooperSurgical, Inc.

Recalled Item: CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D Recalled by...

The Issue: Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2014· ArthroCare Medical Corporation

Recalled Item: Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger...

The Issue: Potential breach of sterile barrier due to defective product tray.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2014· Straumann USA, LLC

Recalled Item: Drill set long Recalled by Straumann USA, LLC Due to Drill set may contain...

The Issue: Drill set may contain incorrect drill.

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

Class II — Potential Health HazardOngoing
FoodOctober 27, 2014· Kent Precision Foods Group, Inc.

Recalled Item: Chicken flavored broth base and seasoning Recalled by Kent Precision Foods...

The Issue: Orrington Farms Chicken Flavored Broth Base & Seasoning, Low Sodium labels...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 24, 2014· Discus Dental LLC

Recalled Item: Relief ACP Oral Care Gel intended to relieve discomfort from Recalled by...

The Issue: Product sold after April 1, 2014 were inadvertently filled with hydrogen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2014· Integra LifeSciences Corp.

Recalled Item: Integra Titan Reverse Shoulder System right and left head cutting templates...

The Issue: A single lot of left and a single lot of right Reverse Shoulder System...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2014· AGFA Healthcare Corp.

Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some...

The Issue: Some material of the coating Type CXCPMV3 has potential artifacts showing a...

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

Class III — Low RiskOngoing
DrugOctober 24, 2014· Hospira Inc.

Recalled Item: Meropenem I.V. 1 g is supplied in 30 mL injection vials Recalled by Hospira...

The Issue: Defective Container: Glass vials may crack due to low (thin) out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2014· CareFusion 213, LLC

Recalled Item: Scrub Care Chlorhexidine Gluconate Solution Recalled by CareFusion 213, LLC...

The Issue: Does Not Meet Monograph: Chlorhexidine Gluconate Surgical Scrub Brush is...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 23, 2014· Data Innovations, LLC

Recalled Item: JResultNet drivers using ASTM coding language. Calculator/data processing...

The Issue: Software issue resulting in the results of one patient potentially being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Medtest Holdings, Inc.

Recalled Item: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) Recalled by...

The Issue: MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2...

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

Class III — Low RiskOngoing
Medical DeviceOctober 23, 2014· Abbott Molecular

Recalled Item: Abbott m2000sp Recalled by Abbott Molecular Due to Some versions of...

The Issue: Some versions of Application Specifications (App Spec) are incompatible with...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2014· Remel Inc

Recalled Item: Oxoid Legionella Latex Test Recalled by Remel Inc Due to A reagent within...

The Issue: A reagent within the test may return false negative results.

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

Class II — Potential Health HazardOngoing