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. 2,423 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,423 in last 12 months

Showing 3102131040 of 50,117 recalls

DrugJanuary 27, 2017· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Mirtazapine Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablets...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 27, 2017· Maquet Cardiovascular, LLC

Recalled Item: VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage:...

The Issue: Maquet has received several complaints involving the VASOVIEW HEMOPRO...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2017· Becton Dickinson & Company

Recalled Item: BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride 14.4 mg...

The Issue: After a receiving a customer complaint for incorrect labeling, BD has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2017· Radiometer America Inc

Recalled Item: ABL90 Flex Model #: 393-090 Portable Recalled by Radiometer America Inc Due...

The Issue: Reports that the sample type "cord blood" has been changed into the two...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2017· Radiometer America Inc

Recalled Item: The ABL800 Model#:All Recalled by Radiometer America Inc Due to Reports that...

The Issue: Reports that the sample type "cord blood" has been changed into the two...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2017· COVIDIEN MEDTRONIC

Recalled Item: Valleylab Laparoscopic Handset Recalled by COVIDIEN MEDTRONIC Due to...

The Issue: Customer reports of the device handset continuing to operate after release...

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

Class II — Potential Health HazardOngoing
FoodJanuary 26, 2017· NSE Products, Inc.

Recalled Item: Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 Recalled...

The Issue: Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 25, 2017· Integra LifeSciences Corp.

Recalled Item: The UNI-CP System Recalled by Integra LifeSciences Corp. Due to The firm...

The Issue: The firm received one complaint from one non-US sales representative...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON KD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON MD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON M 6730/6740 (MEX) Accelerator Recalled by Siemens Medical Solutions...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON M 7400/7440(MEX) Accelerator Recalled by Siemens Medical Solutions...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Quidel Corporation

Recalled Item: Influenza Transport Swab Packages Recalled by Quidel Corporation Due to...

The Issue: Quidel Corporation is recalling Influenza Transport Swab Packages because it...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS HI and Mevatron M2/Primus Mid-Energy Recalled by Siemens Medical...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON M 6700 (MX) Accelerator Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...

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

Class II — Potential Health HazardOngoing
FoodJanuary 24, 2017· Circle U Foods, Inc

Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass inclusion

The Issue: Potential glass inclusion

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 24, 2017· Circle U Foods, Inc

Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...

The Issue: Potential glass inclusion

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 24, 2017· Circle U Foods, Inc

Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...

The Issue: Potential glass inclusion

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 24, 2017· Circle U Foods, Inc

Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...

The Issue: Potential glass inclusion

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 24, 2017· Circle U Foods, Inc

Recalled Item: Circle U Foods Recalled by Circle U Foods, Inc Due to Potential glass...

The Issue: Potential glass inclusion

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

Class II — Potential Health HazardOngoing
Refund