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. 2,464 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,464 in last 12 months

Showing 2100121020 of 50,117 recalls

Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Superset with 22MM ID Recalled by Intersurgical Inc Due to The port may...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Intersurgical Inc

Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...

The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Aesculap Implant Systems LLC

Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM Product Usage: Instrument intended...

The Issue: possibility of the sterility batch being insufficiently sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Integra LifeSciences Corp.

Recalled Item: Integra Jarit GEMINI CLAMP 9 1/4 inch - used in Recalled by Integra...

The Issue: A small crack at the box lock corner may after multiple cleaning and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2019· Aesculap Implant Systems LLC

Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM - Product Usage: Instrument intended...

The Issue: possibility of the sterility batch being insufficiently sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2019· Arrow International Inc

Recalled Item: 8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard Recalled by Arrow...

The Issue: Products may contain the incorrect banner card within the kit

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2019· Preventice Services, LLC

Recalled Item: BodyGuardian Heart Remote Monitoring Kit Recalled by Preventice Services,...

The Issue: The device data being collected and transferred to the monitoring center may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2019· Arrow International Inc

Recalled Item: Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Recalled by...

The Issue: Products may contain the incorrect banner card within the kit

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

Class II — Potential Health HazardOngoing
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Short Fill: fill...

The Issue: Short Fill: fill volume was out of specification at 94 mL (specification: no...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2019· Amys Kitchen Inc

Recalled Item: Amy's Bowls - Broccoli & Cheddar Bake Recalled by Amys Kitchen Inc Due to...

The Issue: Consumer complaints of black plastic found in product.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 5, 2019· Belfonte Ice Cream & Dairy Foods Co

Recalled Item: FROZEN VAN YOG Recalled by Belfonte Ice Cream & Dairy Foods Co Due to...

The Issue: Undeclared allergens peanuts: Peanut butter ice cream was placed in...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2019· PreGel America, Inc.

Recalled Item: PreGel Lemon 50 4.4 lb (2kg) bag Recalled by PreGel America, Inc. Due to...

The Issue: Undeclared Milk. The firm received a complaint that there was milk in the...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 1, 2019· BIMBO Bakeries USA Inc.

Recalled Item: Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Recalled...

The Issue: Possible presence of small plastic pieces caused by a manufacturing failure.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2019· GN Otometrics

Recalled Item: Gold Cup Leadwire and Snap Leadwire with the following component Recalled by...

The Issue: The electrode lead connector has a protruding conductor beyond insulation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2019· Aerolase Corporation

Recalled Item: LightPod Neo Lasers Recalled by Aerolase Corporation Due to This relates to...

The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2019· Rocket Medical Plc

Recalled Item: Rocket KCH Fetal Bladder Drainage Catheter Model: R57405 Recalled by Rocket...

The Issue: A complaint was received regarding kinking of the device prior to use. If a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2019· Aerolase Corporation

Recalled Item: LightPod ERA lasers Recalled by Aerolase Corporation Due to This relates to...

The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...

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

Class II — Potential Health HazardOngoing