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. 2,654 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,654 in last 12 months

Showing 3554135560 of 55,713 recalls

DrugSeptember 15, 2016· Pfizer Inc.

Recalled Item: PREMARIN (conjugated estrogen tablets Recalled by Pfizer Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Bottles were incorrectly...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 15, 2016· Ferrara Candy Comp

Recalled Item: BRACH'S Chocolate Creations Recalled by Ferrara Candy Comp Due to Undeclared...

The Issue: Undeclared peanuts and wheat in product.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 15, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Chemistry 1 Calibrator The Chemistry 1 Calibrator (KC110B)...

The Issue: Siemens determined that discrepant low calcium recovery of QC and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2016· Keystone Dental Inc

Recalled Item: Keystone Dental PrimaConnex¿ Straight Implant TC Recalled by Keystone Dental...

The Issue: Small diameter (SD) cover screw was packaged with the regular diameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2016· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse PACS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...

The Issue: Image data for a patients image may not be correct

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2016· Hand Biomechanics Lab Inc

Recalled Item: Agee-WristJack¿ Fracture Reduction System Recalled by Hand Biomechanics Lab...

The Issue: A number of Agee WristJack¿ Fracture Reduction Systems have been...

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

Class II — Potential Health HazardOngoing
DrugSeptember 13, 2016· Teva Pharmaceuticals USA

Recalled Item: mitoXANTRONE Injection USP (concentrate) Recalled by Teva Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: potential failure to meet the...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 13, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 13, 2016· TEM Systems Inc

Recalled Item: ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US...

The Issue: Customers complained of low/empty reagent vials.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2016· Tearscience, Inc

Recalled Item: LipiFlow thermal Pulsation System Recalled by Tearscience, Inc Due to...

The Issue: Complaints related to an error condition occurring during patient treatment...

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2016· MOORE'S COMPOUNDING PHARMACY

Recalled Item: Levothyroxine Sodium 135 mcg/Liothyronine 15 mcg SR capsules Recalled by...

The Issue: Superpotent Drug and Subpotent Drug; potency failures obtained

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 12, 2016· Safecor Health, LLC

Recalled Item: Safecor Vitamin B-1 (THIAMINE) 100 mg tablets NDC: 48433-0108-01 Distributed...

The Issue: Box labeled Thiamine Hydrochloride instead of Thiamine Mononitrate

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 12, 2016· A & D Enginering Inc

Recalled Item: Blood Pressure Monitor UA-767PBT-Ci for small cuff. Designed to be Recalled...

The Issue: A&D may have shipped blood pressure monitors that were not labeled for use...

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

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2016· Pfizer Inc.

Recalled Item: Cytotec (misoprostol) Tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradations Specifications; Out of specification results...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 9, 2016· Bio-Botanica, Inc.

Recalled Item: Liquid VITAMIN D-3 Drops distributed under the following private labels...

The Issue: The lots exceed the label claim for Vitamin D3 of 2000 IU per drop.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2016· Censea Inc

Recalled Item: A-PAC Farm Raised Shrimp Recalled by Censea Inc Due to Potential Salmonella...

The Issue: Salmonella detected in product

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 9, 2016· Censea Inc

Recalled Item: A-PAC Farm Raised Shrimp Recalled by Censea Inc Due to Potential Salmonella...

The Issue: Salmonella detected in product

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 9, 2016· Teleflex Medical

Recalled Item: Teleflex Percuaneous Solutions Recalled by Teleflex Medical Due to The...

The Issue: The product is being recalled due to a labeling error. The Gripper Graspers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Contour Fabricators Inc

Recalled Item: Zero-Gravity Radiation Protection System Radiology Personnel protective...

The Issue: Two customer complaints suggest that excessive rotation of the cable in one...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Teleflex Medical

Recalled Item: Teleflex Percuaneous Solutions Recalled by Teleflex Medical Due to The...

The Issue: The product is being recalled due to a labeling error. The Gripper Graspers...

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

Class II — Potential Health HazardOngoing