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. 1,129 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,129 in last 12 months

Showing 2161–2180 of 50,117 recalls

DrugJune 16, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: An out of specification results observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 16, 2025· Qualgen, LLC

Recalled Item: Testosterone 200 mg Pellet packaged in 1mL amber vials Recalled by Qualgen,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 16, 2025· Draeger, Inc.

Recalled Item: HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter....

The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: SwabFlush Prefilled Syringe with ICU Medical SwabCaps Recalled by MEDLINE...

The Issue: SwabFlush syringes are affected by the ICU Medical recall of their SwabCap...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2025· Volcano Corp

Recalled Item: Volcano Visions Digital IVUS Catheter: PV.014P (Platinum) Recalled by...

The Issue: Reports of IVUS catheter and guide wire entanglement during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2025· Immunotech A.S.

Recalled Item: Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA...

The Issue: Estrone RIA kit lots may rarely give falsely high patient results which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2025· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL Recalled by Johnson & Johnson Vision...

The Issue: Due to defects (bubbles/voids) identified during standard finished goods testing

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 Recalled by...

The Issue: Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· FUJIFILM Healthcare Americas Corporation

Recalled Item: ASPRIRE Cristalle Mammography System (cleared under K212873) installed with...

The Issue: Devices had an unapproved slabbing software function enabled for use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· RECORDATI RARE DISEASES INC.

Recalled Item: Caphosol Artificial Saliva (32 doses sachet box). 64 x 15 Recalled by...

The Issue: Out of specification stability test result for the Caphosol B solution from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray Recalled by...

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
DrugJune 11, 2025· Macleods Pharmaceuticals Ltd

Recalled Item: Famciclovir Tablets Recalled by Macleods Pharmaceuticals Ltd Due to Presence...

The Issue: Presence of Foreign Substance- Black hair strand found attached to a tablet...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV....

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
FoodJune 11, 2025· Vita Warehouse Corp.

Recalled Item: 1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Recalled by Vita...

The Issue: Contains undeclared peanut

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System...

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Foundation For Sight

Recalled Item: BostonSight SCLERAL Lens Recalled by Boston Foundation For Sight Due to...

The Issue: Select orders of lenses were manufactured with errors impacting sagittal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Foundation For Sight

Recalled Item: BostonSight PROSE Lens. Recalled by Boston Foundation For Sight Due to...

The Issue: Select orders of lenses were manufactured with errors impacting sagittal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing