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. 2,335 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,335 in last 12 months

Showing 4536145380 of 50,117 recalls

Medical DeviceJuly 8, 2013· Sorin Group USA, Inc.

Recalled Item: Edwards Lifesciences Suction Wand Model S099B Recalled by Sorin Group USA,...

The Issue: Sorin Group is recalling certain lots of Edwards Lifesciences Suction Wand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Mullins Transseptal Adult 7F Recalled by Medtronic Inc. Cardiac...

The Issue: Medtronic identified a specific labeling issue for specific lots of Mullins...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Philips Healthcare Inc.

Recalled Item: Radiohead Access Point 1.4 GHz Radiohead Access Point Firmware versions:...

The Issue: IntelliVue Smart-hopping 1.4 GHz Access Point may experience unexpected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2013· Radiometer America Inc

Recalled Item: pCO2 D788 Membranes. Distributed by Radiometer America Recalled by...

The Issue: RADIOMETER has become aware that some D788 pCO2 membranes can cause biased...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: The patient support may move in an unintended manner if the footswitch cover...

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

Class II — Potential Health HazardOngoing
DrugJuly 4, 2013· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurites/Degradation Specifications: Test failure of single largest...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 4, 2013· Whole Foods Market

Recalled Item: Crave Brothers Les Freres cheese sold with labeling as: Les Freres Recalled...

The Issue: Whole Foods Market announces that it is recalling Crave Brothers Les Freres...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 3, 2013· Procter & Gamble Co

Recalled Item: DayQuil Sinex DayTime Sinus Relief (acetaminophen 325 mg and phenylephrine...

The Issue: Unit Dose Mispackaging: Product packaging defect which could result in code...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 3, 2013· NOW Foods

Recalled Item: White plastic bottle with blue cap containing 90 capsules Recalled by NOW...

The Issue: It has been determined that this product contains an undeclared ingredient,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2013· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Reservoirs Recalled by Medtronic MiniMed Due to...

The Issue: Medtronic is recalling certain lots of Medtronic MiniMed Paradigm Reservoirs...

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

Class II — Potential Health HazardOngoing
DrugJuly 2, 2013· Core Pharma Llc

Recalled Item: Pyridostigmine Bromide Tablets 60 mg Recalled by Core Pharma Llc Due to...

The Issue: Failed Stability Specifications: Pyridostigmine Bromide tablets, is being...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 2, 2013· Somersault Snack Co., LLC

Recalled Item: Somersault Pacific Sea Salt flavor Recalled by Somersault Snack Co., LLC Due...

The Issue: A limited number of packages of 1 ounce Somersault Pacific Sea Salt products...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER W/ GEL Recalled by...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER Recalled by Ecolab Inc...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL Recalled by Ecolab...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER Recalled by Ecolab Inc Due...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL Recalled by Ecolab...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Ecolab Inc

Recalled Item: MICROTEK(TM) MEDICAL BUR HOLE LATEX FREE PROBE COVER WITH GEL Recalled by...

The Issue: Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Elekta, Inc.

Recalled Item: Monaco RTP System Radiation treatment planning Recalled by Elekta, Inc. Due...

The Issue: Upgrade installation script is designed to overwrite the same pouch files in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp...

The Issue: Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.

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

Class II — Potential Health HazardOngoing