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. 2,048 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,048 in last 12 months

Showing 64816500 of 50,117 recalls

Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion manual surgical kits labeled as: a) ST. VIRTUS SPLINTER Recalled...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion manual surgical kits labeled as: a) SUTURE REMOVAL TRAY Recalled...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion scalpel handle kits labeled as: a) STERILE # 3 SCALPEL HANDLE...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Manual surgical kits labeled as: a) 15ML SAMPLING TUBE WITH CAP...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Maple Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion Curette kits labeled as: a) STERILE BUCK EAR CURETTE "00" (25697)...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Human Care Hc Sweden Ab

Recalled Item: Altair 330 lbs w/o Hanger Bar Recalled by Human Care Hc Sweden Ab Due to...

The Issue: Patient lift hanger bar may come loose, which could potentially pose risks...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE SWABSTICKS PVP 3 PK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Software Version Numbers version numbers 8B Recalled by RAYSEARCH...

The Issue: A use error that has occurred with RayStation/RayPlan, where material...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion manual surgical kits labeled as: a) STERILE 4-1/2" S/S Recalled by...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion DISP.UMBILICAL CORD CLAMP CUTTER(CTR300) Recalled by MEDLINE...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

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

Class II — Potential Health HazardOngoing
FoodFebruary 23, 2024· Backstage Center DBA CTC Seller

Recalled Item: Alipotec Raiz de Tejocote dietary supplements Recalled by Backstage Center...

The Issue: The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation 4000 . Intended to securely store Recalled by CareFusion...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES (Med ES Main) . Intended Recalled by CareFusion 303,...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation Auxiliary ES . Intended to securely Recalled by...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation Auxiliary 4000 . Intended to securely Recalled by...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Magellan Diagnostics, Inc.

Recalled Item: The LeadCare¿ II Blood Lead Test System relies on electrochemistry Recalled...

The Issue: Calibration Buttons being used in the kitting process were incorrectly...

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

Class II — Potential Health HazardOngoing
DrugFebruary 22, 2024· Eugia US LLC

Recalled Item: Tobramycin for Injection Recalled by Eugia US LLC Due to Failed Stability...

The Issue: Failed Stability Specification: Water determination was found not complying...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing