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. 2,370 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,370 in last 12 months

Showing 4176141780 of 50,117 recalls

DrugJuly 30, 2014· Pfizer Inc.

Recalled Item: Depo-Medrol (methylprednisolone acetate injectable suspension USP) Recalled...

The Issue: Failed pH Specification: A pH result of 2.9 was obtained at the 9 month...

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

Class III — Low RiskOngoing
Refund
DrugJuly 30, 2014· Novartis Pharmaceuticals Corp.

Recalled Item: Cataflam (diclofenac potassium) tablets Recalled by Novartis Pharmaceuticals...

The Issue: Failed Tablet/Capsule Specifications: Ink identification had rubbed off...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM Recalled by Wright Medical...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW 3.5mm PLATE CHARLOTTE F&A SYSTEM Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Wright Medical Technology, Inc.

Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...

The Issue: Plates manufactured from an incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2014· Zimmer, Inc.

Recalled Item: Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral...

The Issue: Internal review found that five (5) PFJ implant forgings were identified as...

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

Class II — Potential Health HazardOngoing
DrugJuly 29, 2014· Hospira Inc.

Recalled Item: Lidocaine HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: The product was discolored and contained...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 29, 2014· Super Organic Foods, Inc

Recalled Item: Sunburst SUPERFOODS ORGANIC RAW CAROB POWDER in ONE POUND and Recalled by...

The Issue: The repacked product has the potential to be contaminated with Salmonella...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 28, 2014· Boehringer Ingelheim Roxane Inc

Recalled Item: OXYCODONE HYDROCHLORIDE C II Oral Solution USP Recalled by Boehringer...

The Issue: Failed Stability Specifications: Out of specification result for...

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

Class III — Low RiskOngoing
Refund
FoodJuly 28, 2014· Swanson Health Products, Inc

Recalled Item: Swanson 100% Certified Organic Recalled by Swanson Health Products, Inc Due...

The Issue: Swanson Certified Organic Carob Powder, item number SWF115 is being recalled...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 28, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: The Symbia T Series consists of the T16 Recalled by Siemens Medical...

The Issue: Siemens Medical Solutions USA, Inc. is performing a field correction because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: The Symbia Intevo series consists of the Intevo 16 Recalled by Siemens...

The Issue: Siemens Medical Solutions USA, Inc. is performing a field correction because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Minstrel (with scale) Product Usage: is a mobile passive hoist. Recalled by...

The Issue: ArjoHuntleigh received three reports where the bolt under the scale...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2014· Becton Dickinson & Co.

Recalled Item: BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen...

The Issue: These lots of Agar may have exhibited breakthrough growth of vancomycin...

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

Class II — Potential Health HazardOngoing