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 2348123500 of 50,117 recalls

FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: RXBAR: Coffee Chocolate Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: KIDS Berry Blast Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to Undeclared...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: RXBAR: Apple Cinnamon Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: RXBAR: 12-Bar Variety Pack (Chocolate Sea Salt Recalled by CHICAGO BAR...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: RXBAR: Chocolate Chip Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: RXBAR: Maple Sea Salt Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: RXBAR: 10-Bar Variety Pack (Blueberry Recalled by CHICAGO BAR COMPANY LLC...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Associates of Cape Cod, Inc.

Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...

The Issue: The kits may contain the incorrect number of components or the kits may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Real Feel Recalled by Reckitt Benckiser LLC Due to Five batches of the...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Boston Scientific Corporation

Recalled Item: Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch...

The Issue: A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Cincinnati Sub-Zero...

The Issue: Evidence supports that when customers performed a fuse replacement as part...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT (non-RoHS) Recalled by Philips Medical Systems...

The Issue: A software update is being issued to correct multiple issues identified in...

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

Class II — Potential Health HazardOngoing
DrugDecember 19, 2018· Teva Pharmaceuticals USA

Recalled Item: Olmesartan Medoxomil and Hydrochlorothiazide Tablets Recalled by Teva...

The Issue: Failed dissolution specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 18, 2018· Insulet Corporation

Recalled Item: Omnipod DASH Insulin Management System Recalled by Insulet Corporation Due...

The Issue: There is a potential for a communication interruption following a bolus...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: "J" Type Bone Marrow Needle 11ga x 10 cm - Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Double Diamond J Type Bone Marrow Needle & Marrow Extraction Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing