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. 2,404 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,404 in last 12 months

Showing 3526135280 of 50,117 recalls

Medical DeviceJanuary 11, 2016· Zimmer Biomet, Inc.

Recalled Item: Gender PFJ FEMORAL COMP Recalled by Zimmer Biomet, Inc. Due to LDPE bag...

The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Varian Medical Systems, Inc.

Recalled Item: Eclipse Treatment Planning System versions 11 Recalled by Varian Medical...

The Issue: When using PBC 11.0.31 to calculate the dose for a conventional arc field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Enzymatic Creatinine CP ref. A11A01907 reagent is intended...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic Recalled...

The Issue: Blade exhibiting fracture during hip arthroscopy procedures

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Glucose PAP CP ref. A11A01668 reagent is intended Recalled by...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: The ABX PENTRA Cholesterol CP ref. A11A01634 is an in Recalled by Horiba...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Lactic Acid CP ref. A11A01721 reagent is intended Recalled by...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Uric Acid CP ref. A11A01670 is an in Recalled by Horiba...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Triglycerides CP ref. A11A01640 is an in vitro Recalled by Horiba...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
DrugJanuary 11, 2016· Pfizer Inc.

Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...

The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2016· Pfizer Inc.

Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...

The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bull's Genital Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Super Hard Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bigger Longer More Time More Sperms Recalled by R Thomas Marketing, LLC Due...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Black Ant King Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Plant Vigra Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Man King Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bull Recalled by R Thomas Marketing, LLC Due to Marketed Without An Approved...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Samurai-X Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Night Man Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund