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. 1,096 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,096 in last 12 months

Showing 21461–21480 of 55,713 recalls

DrugNovember 15, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clobetasol Propionate Foam Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Defective delivery system; product is not foaming or is coming out as liquid.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation) Recalled by Glenmark...

The Issue: Defective delivery system; product is not foaming or is coming out as liquid.

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 15, 2019· Tytek Medical Inc

Recalled Item: PneumoDart Recalled by Tytek Medical Inc Due to A defect involving an...

The Issue: A defect involving an occluded needle was discovered during a training exercise.

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2019· Baxter Healthcare Corporation

Recalled Item: Revaclear Capillary Dialyzer 300 Recalled by Baxter Healthcare Corporation...

The Issue: There is the potential presence of particular matter in the header caps of...

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

Class II — Potential Health HazardOngoing
FoodNovember 15, 2019· THE KRAFT HEINZ COMPANY

Recalled Item: Breakstones 4% Milkfat Large Curd Cottage Cheese Recalled by THE KRAFT HEINZ...

The Issue: Potential presence of pieces of red plastic and metal that may have been...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 15, 2019· SARA LEE FROZEN FOODS

Recalled Item: Chef Pierre 37 Ounce Pumpkin Spice Latte Pie Recalled by SARA LEE FROZEN...

The Issue: undeclared FD & C Red 40

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

Class III — Low RiskOngoing
Refund
FoodNovember 15, 2019· THE KRAFT HEINZ COMPANY

Recalled Item: Breakstones 4% Milkfat Small Curd Cottage Cheese Recalled by THE KRAFT HEINZ...

The Issue: Potential presence of pieces of red plastic and metal that may have been...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 15, 2019· THE KRAFT HEINZ COMPANY

Recalled Item: Breakstones 2% Milkfat Lowfat Large Curd Cottage Cheese Recalled by THE...

The Issue: Potential presence of pieces of red plastic and metal that may have been...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2019· Cardinal Health Inc.

Recalled Item: Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent...

The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Cardinal Health Inc.

Recalled Item: S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent...

The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Cardinal Health Inc.

Recalled Item: Cordis S.M.A.R.T. CONTROL /S.M.A.R.T. Vascular Stent System. The S.M.A.R.T....

The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego Interventional Fluoroscopic X-Ray System Recalled by...

The Issue: In affected Artis zee floor Interventional Fluoroscopic X-Ray Systems, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Abbott Diabetes Care, Inc.

Recalled Item: Optium EZ Blood Glucose Monitoring System Recalled by Abbott Diabetes Care,...

The Issue: Instructions sent in a letter or in instructions for use for disinfecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Abbott Diabetes Care, Inc.

Recalled Item: Precision Xtra Blood Glucose & Ketone Monitoring System Recalled by Abbott...

The Issue: Instructions sent in a letter or in instructions for use for disinfecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Hardy Diagnostics

Recalled Item: HardyCHROM MRSA Recalled by Hardy Diagnostics Due to False Positive results...

The Issue: False Positive results due to the MSSA (methicillin-susceptible) strain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2019· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Precision H Blood Glucose and Ketone Monitoring System Recalled by...

The Issue: Instructions sent in a letter or in instructions for use for disinfecting...

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

Class II — Potential Health HazardOngoing
DrugNovember 14, 2019· AVKARE Inc.

Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2019· AVKARE Inc.

Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2019· Natures Rx

Recalled Item: Silver Bullet Recalled by Natures Rx Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2019· Precision Dose Inc.

Recalled Item: Ranitidine Oral Solution Recalled by Precision Dose Inc. Due to CGMP...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API.

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

Class II — Potential Health HazardOngoing
Refund