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 4632146340 of 50,117 recalls

Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8 mm Monopolar Curved Scissors (a.k.a. Hot Shears) Manufactured and Recalled...

The Issue: Intuitive Surgical has identified a potential for some units of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Maryland Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Fenestrated Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Verathon, Inc.

Recalled Item: GlideScope Video Laryngoscope (GVL) 3 Recalled by Verathon, Inc. Due to...

The Issue: Verathon GlideScope Reusable GVL and AVL Blades are being recalled due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2013· SpineFrontier, Inc.

Recalled Item: InSpan Inserter Recalled by SpineFrontier, Inc. Due to Potential for set...

The Issue: Potential for set screw to be come deformed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: The Zimmer Air Dermatome Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
DrugMay 7, 2013· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Topical Oil (SCALP OIL) Recalled...

The Issue: Subpotent Drug: the active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Fiber Drink Mix Recalled by Novartis Consumer Health Due to The...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Fiber Supplement Plus Calcium Recalled by Novartis Consumer Health...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Plus Heart Health Non-Thickening Powder Recalled by Novartis...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Fiber Supplement Recalled by Novartis Consumer Health Due to The...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· Novartis Consumer Health

Recalled Item: Benefiber Non-Thickening Powder Recalled by Novartis Consumer Health Due to...

The Issue: The products are being recalled due to the receipt of a relatively high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 7, 2013· American Importing Co, Inc

Recalled Item: Market Pantry Recalled by American Importing Co, Inc Due to American...

The Issue: American Importing Co, Inc is recalling Market Pantry Sweet & Salty Mix...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 6, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens RAD Fluoro Uro Systems - Luminos dRF Recalled by Siemens Medical...

The Issue: Siemens has discovered through product monitoring a potential malfunction...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: There is evidence that an electrical short within the systems connector has...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) Chemistry Wash (RD701) Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics received complaints of Chemistry Wash causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Fixation Cannula - 5mm Product Code: ONBFCA5ST...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing