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. 927 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
927 in last 12 months

Showing 47021–47040 of 50,117 recalls

Medical DeviceMarch 5, 2013· Stryker Endoscopy

Recalled Item: 1488 HD 3-Chip Inline Camera Recalled by Stryker Endoscopy Due to In certain...

The Issue: In certain operating room environments, a colored screen image occurs with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2013· Stryker Endoscopy

Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...

The Issue: In certain operating room environments, a colored screen image occurs with...

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

Class II — Potential Health HazardOngoing
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: SEPP 2% Iodine Tincture USP (47% v/v Ethyl Alcohol Recalled by CareFusion...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol)...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution)...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: SEPP 10% Povidone Iodine Solution USP (1% available Iodine Recalled by...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: Donor Prep Kit containing 1 FREPP (70% isopropyl alcohol) Recalled by...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2013· CareFusion 213, LLC

Recalled Item: SEPP 70% Isopropanol (isopropyl alcohol) 70% v/v Recalled by CareFusion 213,...

The Issue: Labeling: Not Elsewhere Classified: This product is misbranded because the...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2013· Tri-Union Seafoods, L.L.C dba Chicken of the Sea.

Recalled Item: Chicken of the Sea Brand 5-ounce chunk white albacore tuna Recalled by...

The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2013· Tri-Union Seafoods, L.L.C dba Chicken of the Sea.

Recalled Item: Chicken of the Sea 5-Ounce Chunk Light Tuna in Oil. Recalled by Tri-Union...

The Issue: Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 4, 2013· Medtronic Xomed, Inc.

Recalled Item: x1 NIM TriVantage EMG Endotracheal Tube 5.0 mm Recalled by Medtronic Xomed,...

The Issue: In March 2013, Medtronic issued a recall of the NIM TriVantage EMG...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2013· Steris Corporation

Recalled Item: Quick Connect QLC1677E Recalled by Steris Corporation Due to During a...

The Issue: During a routine label review, the firm identified four SYSTEM 1E Quick...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2013· Arrow International Inc

Recalled Item: Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse...

The Issue: The product specifications sheet, part of the Instructions for Use (IFU),...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2013· CareFusion 213, LLC

Recalled Item: Sepp Recalled by CareFusion 213, LLC Due to An internal review of...

The Issue: An internal review of CareFusion's labeling for preoperative skin prep...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2013· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz Dual series CT Scanner System Recalled by Philips And Neusoft Medical...

The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2013· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Multi-Slice CT Scanner System Recalled by Philips And Neusoft...

The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo.plaza SW version VA20 with Mammography license. image...

The Issue: Siemens issued a Customer Safety Notice to inform customers of a potential...

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

Class II — Potential Health HazardOngoing
DrugMarch 2, 2013· Physicians Total Care, Inc.

Recalled Item: Voltaren 1% Gel Recalled by Physicians Total Care, Inc. Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date; This recall is...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 1, 2013· American Medical Systems, Inc.

Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...

The Issue: American Medical Systems, Inc. is initiating a recall on two components of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir Recalled...

The Issue: Certain lots of Reagent reservoirs, may not have a separation in the lower...

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

Class II — Potential Health HazardOngoing