Product Recalls in Texas

Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,680 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,680 in last 12 months

Showing 2894128960 of 55,713 recalls

Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Premature Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: French Rose Clay Recalled by Plant Devas Inc Due to FDA Office of Colors and...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Lemongrass Facial Polish with Oats Recalled by Plant Devas Inc Due to FDA...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Rose Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of Colors...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Clay Mask Kit Recalled by Plant Devas Inc Due to FDA Office of Colors and...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Blue Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of Colors...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Blemish Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Green Tea Clay Recalled by Plant Devas Inc Due to FDA Office of Colors and...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2018· Plant Devas Inc

Recalled Item: Ayurvedic Face Care Kit Recalled by Plant Devas Inc Due to FDA Office of...

The Issue: FDA Office of Colors and Cosmetics sampled product and found virulent and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2018· Helena Laboratories, Corp.

Recalled Item: SPIFE Alkaline Hemoglobin Kit Recalled by Helena Laboratories, Corp. Due to...

The Issue: Lots of gel kits contained a newer revision of the Customer Procedures...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 27, 2018· Integrity Implants Inc.

Recalled Item: FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System)...

The Issue: Recently Integrity Implants uncovered a discrepancy in the cleaning...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2018· Genesee BioMedical, Inc.

Recalled Item: Sternal Valve Retractors With Atrial and Aortic Rakes Recalled by Genesee...

The Issue: Failure in a retractor blade due to corrosion. In the area of the blade...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2018· Beaver-Visitec International Inc.

Recalled Item: Wet-Field Hemostatic Eraser Bipolar 25G Recalled by Beaver-Visitec...

The Issue: Products were packaged with incorrect labeling,

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2018· Mckesson Packaging Services

Recalled Item: RANITIDINE Tablets Recalled by Mckesson Packaging Services Due to Failed...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2018· Paddock Laboratories, LLC.

Recalled Item: Evamist (estradiol transdermal spray) Recalled by Paddock Laboratories, LLC....

The Issue: Defective Delivery System: Potential that cracks in the vial neck near the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2018· AstraZeneca Pharmaceuticals LP

Recalled Item: Lynparza (olaparib) capsules 50 mg Recalled by AstraZeneca Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications; elevated levels of quality...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 23, 2018· Civco Medical Instruments Co. Inc.

Recalled Item: CIVCO lnfiniti Needle Guide Bracket. used for performing needle-guided (or...

The Issue: A cover failed leak testing during validation testing of new needle guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· ConMed Corporation

Recalled Item: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...

The Issue: Wire sets of certain devices were assembled with adhesive on the contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: 12F X 40CM TESIO CATHETER SET WITH "Y" ADAPTOR Recalled by Medical...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2018· Medical Components, Inc dba MedComp

Recalled Item: 12F Tesio CATHETER SET (CUFF 32CM FROM TIP) Recalled by Medical Components,...

The Issue: There is the potential for connection failures related to the female...

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

Class II — Potential Health HazardOngoing