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. 2,334 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,334 in last 12 months

Showing 4640146420 of 50,117 recalls

Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar Standard. Designed to meet the needs for lifting humans. Recalled...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: EZ Breathe Medication Cup. For the delivery of liquid medications Recalled...

The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2013· Angiodynamics, Inc.

Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...

The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: EZ Breathe Atomizer Model # EZ-100. For the delivery of Recalled by Nephron...

The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2013· TZ Medical Inc.

Recalled Item: adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is...

The Issue: TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· American Optisurgical Inc

Recalled Item: TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1...

The Issue: American Optisurgical, Inc. is recalling certain lots of TX1 Tissue Removal...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· American Optisurgical Inc

Recalled Item: FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray....

The Issue: American Optisurgical, Inc initiated a recall of ChloraPrep Hi-Lite Orange...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar 350. Designed to meet the needs for lifting humans. Recalled by...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Elekta, Inc.

Recalled Item: Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated...

The Issue: Unexpected movement during beam delivery may not be detected if there are...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one...

The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2013· Angiodynamics, Inc.

Recalled Item: AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following...

The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar 360. Designed to meet the needs for lifting humans. Recalled by...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· Hospira Inc.

Recalled Item: DOBUTamine in 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Confirmed report of leaking in the primary...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2013· King Legacy, a wholly owned subsidiary of Pfizer

Recalled Item: Levoxyl (levothyroxine sodium) tablets Recalled by King Legacy, a wholly...

The Issue: Subpotent Drug: The products were below specification for potency at the...

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

Class II — Potential Health HazardOngoing
Refund