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. 2,440 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,440 in last 12 months

Showing 2282122840 of 50,117 recalls

DrugApril 2, 2019· Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Recalled Item: Vancomycin 125 mg/3mL Inhalation Recalled by Anderson Compounding Pharmacy,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Dornier Medtech America, Inc.

Recalled Item: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers...

The Issue: Pin hole package failures compromising sterility of product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Zimmer Biomet, Inc.

Recalled Item: Mobi-C 14mm Distraction Screw Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Incorrect part description contained on an additional label placed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Olympus Corporation of the Americas

Recalled Item: Olympus MAJ-209 Single Use Suction Valves Recalled by Olympus Corporation of...

The Issue: There is a potential for the single use suction valve to come apart and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2019· Teleflex Medical

Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...

The Issue: The firm received reports indicating that the laser guard foil partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2019· Integra Limited

Recalled Item: Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra...

The Issue: Stability did not meet acceptance criteria for visual appearance during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2019· Verathon, Inc.

Recalled Item: GlideScope Video Laryngoscope Recalled by Verathon, Inc. Due to A...

The Issue: A typographical error in the Operations & Maintenance Manual incorrectly...

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

Class II — Potential Health HazardOngoing
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Classic Herb Bread Mix 19oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Black Bean Brownie Mix 14oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Dairy & Corn Free Bread Mix 19oz Recalled by Wholesome...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Yeast Free Bread Mix 18.1oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Banana Bread Mix 14oz Recalled by Wholesome Treats, Inc....

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 30, 2019· LITTLE RED ROOSTER COMPANY

Recalled Item: NadaMoo! Strawberry Cheesecake Non-Dairy Frozen-Dessert 16 ounce/pint...

The Issue: Undeclared almonds

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 30, 2019· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to...

The Issue: Outflow Graft leaking at the pump connection during the implantation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2019· Thoratec Corp.

Recalled Item: Thoratec Heartmate 3 Sealed Outflow Graft with Bend Relief Recalled by...

The Issue: Outflow Graft leaking at the pump connection during the implantation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Precision 500D The Precision 500D R&F X-ray System is intended Recalled by...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing