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. 2,348 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,348 in last 12 months

Showing 4198142000 of 50,117 recalls

DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Methylcobalamin Injection USP 1000 mcg/ml Recalled by Medical...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Super MIC B Complex for L-Carnitine for Injection USP with Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: L-Carnitine Injection USP 100 mg/ml Recalled by Medical Supply Liquidators...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B6 Pyridoxine HCL for Injection USP Recalled by Medical Supply...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Glutathione Injection USP Recalled by Medical Supply Liquidators Llc Due to...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: BCAA 4% Branched Chain Amino Acid Injection USP Recalled by Medical Supply...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 24, 2014· Doctor's Best, Inc.

Recalled Item: Doctor's Best Red Yeast Rice 1200 Recalled by Doctor's Best, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis discovered undeclared...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 24, 2014· Bard Access Systems

Recalled Item: Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter...

The Issue: Potential for inadvertent scalpel stick injury involving the safety scalpel.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Surgical System Console Recalled by Stryker Instruments...

The Issue: The firm received complaints regarding insufficient irrigation to the tip of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2014· Invacare Corporation

Recalled Item: MK5 NX Controller--Wheelchair controller Recalled by Invacare Corporation...

The Issue: M41 Powered Wheelchairs received through Invacare Service Parts (ISP) have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· Laser Peripherals LLC

Recalled Item: LP Recalled by Laser Peripherals LLC Due to Mislabeling

The Issue: Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· Stryker Endoscopy

Recalled Item: Disposable StrykeFlow Tip Recalled by Stryker Endoscopy Due to Internal...

The Issue: Internal review found that six lots of Disposable StrykeFlow Tips were...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Tolterodine Tartrate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugJune 20, 2014· Novel Laboratories, Inc.

Recalled Item: Famotidine for Oral Suspension Recalled by Novel Laboratories, Inc. Due to...

The Issue: Failed Impurity/Degradation Specification; 12-month stability time point

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 20, 2014· ORIGIO, Inc

Recalled Item: Name: Pasteur Pipets Recalled by ORIGIO, Inc Due to Identification of...

The Issue: Identification of packaging breach of the nylon pouch sterile barrier for...

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

Class II — Potential Health HazardOngoing
DrugJune 19, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Pfizer Inc.

Recalled Item: Cardura XL (doxazosin mesylate extended release tablets Recalled by Pfizer...

The Issue: Failed Impurities/Degradation Specifications: Product from this lot may not...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Mckesson Packaging Services

Recalled Item: Aspirin DR Enteric Coated Tablets Recalled by Mckesson Packaging Services...

The Issue: Failed Dissolution Specification; at the 12 month time interval.

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

Class III — Low RiskOngoing
Refund