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. 2,603 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,603 in last 12 months

Showing 67816800 of 50,117 recalls

FoodJanuary 11, 2024· Rizo Lopez Foods, Inc. dba Don Francisco Cheese

Recalled Item: Tio Francisco Recalled by Rizo Lopez Foods, Inc. dba Don Francisco Cheese...

The Issue: Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 11, 2024· Amerisource Health Services LLC

Recalled Item: Rifampin Capsules USP Recalled by Amerisource Health Services LLC Due to...

The Issue: Failed Impurities/Degradation Specification.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2024· Par Sterile Products LLC

Recalled Item: Vasostrict (vasopressin in 5% Dextrose) Injection Recalled by Par Sterile...

The Issue: Superpotent Drug: Assay from the 3-month and 6-month stability intervals...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 11, 2024· Micro Therapeutics, Inc.

Recalled Item: The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible Recalled...

The Issue: European version of microcatheter were distributed within US which contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Micro Therapeutics, Inc.

Recalled Item: The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible Recalled...

The Issue: European version of microcatheter were distributed within US which contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Brasseler USA I Lp

Recalled Item: Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023 Recalled by Brasseler...

The Issue: The device has a grip detail (right angle latch) out of specification...

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

Class II — Potential Health HazardOngoing
FoodJanuary 10, 2024· Now Foods

Recalled Item: Protocol for Life Balance Recalled by Now Foods Due to Amount of...

The Issue: Amount of Phosphatidyl Serine in product is less than stated on the label

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

Class III — Low RiskOngoing
Refund
DrugJanuary 10, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Remedy Clinical TREAT Antifungal Cream Recalled by MEDLINE...

The Issue: Labeling: Not Elsewhere Classified; Product labeling contains the claim of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2024· BE PHARMACEUTICALS AG

Recalled Item: Fosaprepitant for Injection 150 mg per vial Recalled by BE PHARMACEUTICALS...

The Issue: Lack of Sterility Assurance: Aseptic process simulation failure.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 10, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse PACS - Version 7.2.100 Recalled by FUJIFILM Healthcare Americas...

The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...

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

Class II — Potential Health HazardOngoing