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. 2,451 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,451 in last 12 months

Showing 2208122100 of 50,117 recalls

DrugMay 20, 2019· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 20, 2019· Medtronic Inc.

Recalled Item: Guardian Connect App CSS7200 iOS and Guardian Connect Transmitter GST4C...

The Issue: Customers using the firm's continuous glucose monitoring system application...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Opternative Inc

Recalled Item: The Visibly Online Vision Test which is part of Recalled by Opternative Inc...

The Issue: Lack of 510K clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product...

The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product...

The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...

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

Class II — Potential Health HazardOngoing
FoodMay 17, 2019· House of Spices India, Inc.

Recalled Item: Laxmi Brand Dried Apricot 7 oz (200g) Plastic Pouch Code: 2324617054...

The Issue: Product contains elevated levels of undeclared Sulfites

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 17, 2019· U.S. Tov, Inc.

Recalled Item: Global Pride Rattan Shoots in Brine: 24 oz. glass jar Recalled by U.S. Tov,...

The Issue: New York State Department of Agriculture and Markets sampled and tested...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 17, 2019· Arrow International Inc

Recalled Item: Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip...

The Issue: Lidstock contains a labeling error. The lidstock shows the catheter cross...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· GE Healthcare, LLC

Recalled Item: Centricity PACS-IW with Universal Viewer version 5.0 Recalled by GE...

The Issue: There is a potential that one or more images or image series may be missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer with PACS-IW foundation 6.0 Recalled by GE...

The Issue: There is a potential that one or more images or image series may be missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 45 ARTICULATING XTRA THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 45MM MEDIUM/ THIC Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 30MM MEDIUM/ THICK RELOAD Recalled by Covidien LLC Due...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 45 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 30 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 60MM EXTRA THICK RELOA Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 CURVED TIP ART MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 ARTICULATING EXTRA THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 45MM EXTRA THICK RELOA Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing