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. 1,886 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,886 in last 12 months

Showing 2050120520 of 28,538 recalls

Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Uniqcot 1/2" x 1/2" : 67-06 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 3/8" x 2" : 20-26S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 1/2" x 1/2" : 20-04S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 70 mm x 10090 mm : Recalled by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 1/2" x 3" : 60-09 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 15 mm x 15 mm (Glassine) by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Policot 1/2" x 1/2" : 90-06 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cotton Balls-Strung 1/2" : 30-02 Product Usage: Recalled...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cotton Balls-Strung 3/4" : 30-03 Product Usage: Recalled...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 1/2" x 1.5" : 20-06S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Hologic, Inc

Recalled Item: CF InPlex ASR Card Recalled by Hologic, Inc Due to Complaints of false...

The Issue: Complaints of false positive HET mutations and leaking cards; could lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Hologic, Inc

Recalled Item: Hologic InPlex CF Molecular Test (IVD) Recalled by Hologic, Inc Due to...

The Issue: Complaints of false positive HET mutations and leaking cards; could lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Shimadzu Medical Systems

Recalled Item: X-Ray Diagnostic Table Recalled by Shimadzu Medical Systems Due to Report of...

The Issue: Report of unintentional movement of table to reverse tilting.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Biocare Medical, LLC

Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...

The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...

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

Class III — Low RiskOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 5 mm x 8 mm (Glassine) by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: E.cam or Symbia systems that use foresight detectors - Product Recalled by...

The Issue: E. CAM and Symbia system with foresight detectors performing gated or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur CP Immunoassay System Recalled by Siemens Healthcare...

The Issue: The firm identified an issue in sample processing when using EZee-Nest...

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

Class III — Low RiskOngoing
Medical DeviceMarch 30, 2016· Teleflex Medical

Recalled Item: Pleur-evac Chest Drainage System Recalled by Teleflex Medical Due to The...

The Issue: The label on the Tyvek bag is missing. This is used by customers to identify...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...

The Issue: If images are sent without an order in the system, they will be matched with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is voluntarily implementing a Medical Device Recall of one...

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

Class II — Potential Health HazardOngoing