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 66016620 of 50,117 recalls

Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 6 10 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 3 10 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 7 9 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 6 11 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 with a Certeray generator-To perform image guidance in diagnostic...

The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 3 with a Certeray generator -To perform image guidance in diagnostic...

The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 5 with a Certeray generator-To perform image guidance in diagnostic...

The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...

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

Class II — Potential Health HazardOngoing
DrugFebruary 5, 2024· Super Chill Products

Recalled Item: Neptune's Fix Recalled by Super Chill Products Due to Marketed without an...

The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 5, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Mesalamine Extended-Release Capsules Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: Out of specification for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 5, 2024· Abbott Medical

Recalled Item: Abbott Aveir Leadless Pacemaker Recalled by Abbott Medical Due to Their is a...

The Issue: Their is a potential that electromagnetic interference may cause leadless...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2024· Retractable Technologies, Inc.

Recalled Item: EasyPoint Needle Recalled by Retractable Technologies, Inc. Due to The...

The Issue: The needle cannula of a retractable needle may detach from the needle holder...

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

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2024· Bausch Health Companies, Inc.

Recalled Item: Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1 Recalled by...

The Issue: Subpotent Drug: Out of specification for assay

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with Recalled by...

The Issue: Pack and pouch label is missing the manufacturing and expiration date.

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

Class II — Potential Health HazardOngoing
FoodFebruary 1, 2024· House of Coffee Beans, Inc

Recalled Item: Coffee 5 pound bags Recalled by House of Coffee Beans, Inc Due to potential...

The Issue: potential allergen contact with almonds, pecans and coconut.

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

Class II — Potential Health HazardOngoing
Refund