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 4992149940 of 50,117 recalls

DrugMarch 15, 2011· Luitpold Pharmaceuticals, Inc.

Recalled Item: CONCENTRATED SODIUM CHLORIDE INJECTION Recalled by Luitpold Pharmaceuticals,...

The Issue: Presence of Particulate Matter: In the course of inspecting retention...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 9, 2011· Biomet Spine LLC.

Recalled Item: LANX Recalled by Biomet Spine LLC. Due to Biomet Spine, LLC. announces...

The Issue: Biomet Spine, LLC. announces voluntary recall of Durango Anchored ALIF Plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2011· Ge Healthcare It

Recalled Item: Imagecast PACS is an image management system intended to be Recalled by Ge...

The Issue: In Imagecast PACS versions prior to 3.6.51.01, the estimated magnification...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2011· The Anspach Effort, Inc.

Recalled Item: ****** 3mm Diamond Ball. Used for cutting and shaping bone. Recalled by The...

The Issue: Due to three batches of product may have diamond grit size larger than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2011· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-Ray System Recalled by Philips Medical...

The Issue: Multiple software defects which could impact the performance or reliability...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardioplegia Delivery Set- Catalog Number:165720 and Catalog...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Integrated Cardioplegia Delivery Set-LINE FOR 15501/16015/5852...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardioplegia Delivery Set - Heat Exchanger Cardiopulmonary...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Cardioplegia Delivery Set- Item Number: 16130 Product Usage: The...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular and Perfusion Procedure Kits Catalog Codes:...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2011· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardioplegia Delivery Sets Catalog Code: 204880 Product Usage:...

The Issue: Defect in the luer connector can compromise the seal on the female side of...

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

Class II — Potential Health HazardOngoing
DrugFebruary 10, 2011· Abc Compounding Company Inc

Recalled Item: Earth Force Recalled by Abc Compounding Company Inc Due to Chemical...

The Issue: Chemical Contamination: QS Plus wipes were found to be contaminated with...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 2, 2011· Primus Medical LLC

Recalled Item: AC Powered adjustable hospital bed Recalled by Primus Medical LLC Due to The...

The Issue: The "Retaining washers & Clevis Pins" provided with the AC -powered...

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

Class II — Potential Health HazardOngoing
DrugJanuary 19, 2011· VistaPharm, Inc.

Recalled Item: METOCLOPRAMIDE ORAL SOLUTION Recalled by VistaPharm, Inc. Due to Labeling:...

The Issue: Labeling: Correct Labeled Product Miscart/Mispack: The shipper label...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 18, 2011· Nemschoff Chairs, Inc.

Recalled Item: Nemschooff Recalled by Nemschoff Chairs, Inc. Due to Nemschoff Chairs, Inc....

The Issue: Nemschoff Chairs, Inc. is recalling various model of the Serenity Treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing