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. 2,636 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,636 in last 12 months

Showing 32013220 of 50,117 recalls

Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· TAS Medical Inc

Recalled Item: TISSUE APPROXIMATION SYSTEM (TAS) Recalled by TAS Medical Inc Due to Tissue...

The Issue: Tissue approximation straps (zip-ties) have broken before or during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH Recalled...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Dexcom, Inc.

Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...

The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Dexcom, Inc.

Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...

The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Dexcom, Inc.

Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...

The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...

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

Class II — Potential Health HazardOngoing
FoodJanuary 25, 2025· Amazon Retail LLC

Recalled Item: ASIN B0CY2RDW5T Recalled by Amazon Retail LLC Due to Undeclared Egg

The Issue: Undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 25, 2025· Amazon Retail LLC

Recalled Item: ASIN B084PZ7K98 Recalled by Amazon Retail LLC Due to Undeclared Egg

The Issue: Undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2025· SKY PACKAGING

Recalled Item: HydrALAZINE Hydrochloride Recalled by SKY PACKAGING Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2025· SKY PACKAGING

Recalled Item: HydrALAZINE Hydrochloride Recalled by SKY PACKAGING Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 24, 2025· Guangzhou Pluslife Biotech Co., Ltd.

Recalled Item: Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid...

The Issue: Devices were distributed in the U.S. market without obtaining the required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2025· Guangzhou Pluslife Biotech Co., Ltd.

Recalled Item: Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device...

The Issue: Devices were distributed in the U.S. market without obtaining the required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris Pump Module The BD Alaris System Recalled by CareFusion 303, Inc....

The Issue: Due to User Manual/Direction for Use incorrectly instructing user to leave...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedFlex 2.0 Bio-ID Spare Parts by CareFusion 303, Inc. Due to Due...

The Issue: Due to fingerprint scanner failing resulting in the scanner heating up.

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

Class II — Potential Health HazardOngoing
FoodJanuary 22, 2025· La Fiesta Food Products

Recalled Item: La Fiesta PAN RAYADO SAZONADO Bread Crumbs Seasoned Recalled by La Fiesta...

The Issue: Firm distributed a Seasoned Bread Crumb product with undeclared allergen...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2025· La Fiesta Food Products

Recalled Item: La Fiesta PAN RAYADO Bread Crumbs Recalled by La Fiesta Food Products Due to...

The Issue: Firm distributed a Bread Crumb product with undeclared allergen (Sesame) not...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 22, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 22, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lorazepam Tablets Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed impurities/degradation specifications and Sub-potent Drug:...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2025· Provepharm Inc.

Recalled Item: Phenylephrine HCl Injection Recalled by Provepharm Inc. Due to Presence of...

The Issue: Presence of Particulate Matter.

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

Class I — Serious Health HazardOngoing
Refund