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. 2,386 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,386 in last 12 months

Showing 3950139520 of 50,117 recalls

Medical DeviceFebruary 19, 2015· Steris Corporation

Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers Recalled by Steris Corporation Due...

The Issue: STERIS has identified that the control board software in select AMSCO 400...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2015· Steris Corporation

Recalled Item: Caviwave Pro Ultrasonic Cleaning System Recalled by Steris Corporation Due...

The Issue: Should the Caviwave Pro Ultrasonic Cleaning System experience a temporary...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2015· CHG Hospital Beds Inc

Recalled Item: The Spirit TM Select bed is a Med-Surg bed intended Recalled by CHG Hospital...

The Issue: It was identified that in some situations the bed exit alarm may not...

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

Class II — Potential Health HazardOngoing
DrugFebruary 18, 2015· Mylan Institutional LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Lack of Assurance of Sterility; due to leaking vials

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 18, 2015· Mylan Institutional LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Lack of Assurance of Sterility; due to leaking vials

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 17, 2015· King Systems Corp.

Recalled Item: Double Swivel Connector with Suction Port Connector Recalled by King Systems...

The Issue: Product is mislabeled as Double Swivel Connector with Suction Port and is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2015· Synthes, Inc.

Recalled Item: Thumb Screw for the Synthes Recon Locking Aiming Arm for Recalled by...

The Issue: For certain lots, the incorrect raw material of annealed 17-4PH Stainless...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2015· Transonic Systems Inc

Recalled Item: Transonic Hemodialysis Monitor Recalled by Transonic Systems Inc Due to...

The Issue: Customer unable to obtain measurements due to the device seeing no flow or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2015· US Endoscopy Group Inc

Recalled Item: Velocity" Biopsy Valve Recalled by US Endoscopy Group Inc Due to The company...

The Issue: The company has received reports of structural non conformance at the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 16, 2015· West-Ward Pharmaceutical Corporation

Recalled Item: Fentanyl Citrate Inj. Recalled by West-Ward Pharmaceutical Corporation Due...

The Issue: Failed Impurities/Degradation Specifications; 12 month stability testing.

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

Class III — Low RiskOngoing
Refund
FoodFebruary 16, 2015· Unilever United States, Inc.

Recalled Item: Breyers¿ No Sugar Added Salted Caramel Swirl 1.5-quart (1.41L) packaged...

The Issue: Unilever United States, Inc. is voluntarily recalling a limited number of...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 13, 2015· Michael Foods, Inc.

Recalled Item: Natural Shaped Fried Egg (patties) Recalled by Michael Foods, Inc. Due to...

The Issue: Improperly declared milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 13, 2015· Goya Foods, Inc.

Recalled Item: Kirby Black Beans Creole Seasoning Net Wt. 29 oz. Packed for Kirby Foods...

The Issue: Kirby brand black beans with creole seasoning, 29 oz. size and Goya brand...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 13, 2015· Goya Foods, Inc.

Recalled Item: Goya Black Bean Soup Net Wt. 29 oz. Goya Foods Recalled by Goya Foods, Inc....

The Issue: Kirby brand black beans with creole seasoning, 29 oz. size and Goya brand...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2015· Qualitest Pharmaceuticals

Recalled Item: AMLODIPINE BESYLATE TABLETS USP Recalled by Qualitest Pharmaceuticals Due to...

The Issue: Failed tablet specifications: One lot was found to contain oversized tablets.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 13, 2015· Aaren Scientific, Incorporated

Recalled Item: Intraocular Lens (IOL) Recalled by Aaren Scientific, Incorporated Due to...

The Issue: Aaren Scientific is recalling intraocular lenses because the instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2015· Exactech, Inc.

Recalled Item: Equinoxe 44mm Short Humeral Head Catalog Number 310-01-44. Orthopedic...

The Issue: Incorrectly packaged. Outer and inner labeling may incorrectly identify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2015· Medela Inc. EF Division

Recalled Item: - NTL-30 30ml Nutrio Enteral Feeding Syringe (sterile) - NTL-60 Recalled by...

The Issue: The firm is recalling sterile enteral feeding syringes due to determining...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Ameda, Inc.

Recalled Item: Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115)...

The Issue: Devices were not sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Dako North America Inc.

Recalled Item: Autostainer Link 48 (AS480) Recalled by Dako North America Inc. Due to A...

The Issue: A false negative result affecting the diagnosis may occur. A defect in the...

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

Class II — Potential Health HazardOngoing