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. 1,705 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,705 in last 12 months

Showing 4526145280 of 50,117 recalls

Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Tapered Navigator Certain Surgical Kit Product Usage: Molded plastic tray...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Synthes USA HQ, Inc.

Recalled Item: 3.7mm and 5.0mm Dynamic Locking Screw (DLS) Product Usage: 3.7mm Recalled by...

The Issue: All lots of 3.7mm and 5.0mm Dynamic Locking Screw (DLS) were recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· MCKESSON TECHNOLOGIES INC

Recalled Item: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense...

The Issue: The firm issued a clinical alert after users reported an issue where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2013· Biomet 3i, LLC

Recalled Item: Navigator Surgical Kit Product Usage: Molded plastic tray used in Recalled...

The Issue: During recent revised sterilization validation testing, the included...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Edge Mesh (All sizes and shapes). Intended for use Recalled by Atrium...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR V-Patch Mesh (All sizes and shapes). Intended for use Recalled by...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR TacShield Mesh (All sizes and shapes). Intended for use Recalled by...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Blue Belt Technologies MN

Recalled Item: Blue Belt Technologies Recalled by Blue Belt Technologies MN Due to Blue...

The Issue: Blue Belt Technologies is recalling sterile Monitor Drapes used with their...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 300 and ACL TOP 300 CTS (Japan) Recalled by Instrumentation...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Atrium Medical Corporation

Recalled Item: C-QUR Mesh (All Sizes Recalled by Atrium Medical Corporation Due to...

The Issue: Additional Instructions for Use and Storage Conditions as Coated mesh can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2013· Instrumentation Laboratory Co.

Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential carryover issue that can can cause shortened APTT clotting times...

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

Class II — Potential Health HazardOngoing
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Fem Mezcla con L-Carnitina Suplemento Alimenticio Recalled by...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Man Herbal Blend With L-Carnitine Dietary Supplement Recalled by...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Siloutte Suplemento Alimenticio Recalled by Herbal Give Care Llc...

The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2013· Watson Laboratories Inc

Recalled Item: Oxycodone and Acetaminophen Capsules Recalled by Watson Laboratories Inc Due...

The Issue: Subpotent drug: Two lots of Oxycodone and Acetaminophen Capsules, USP 5/500...

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

Class III — Low RiskOngoing
Refund