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. 2,697 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,697 in last 12 months

Showing 2284122860 of 55,713 recalls

DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Tobramycin Irrigation 80 mg/1000 mL Solution Recalled by Wise Pharmacy Due...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine 30 mg/1 mg/mL Injectable Recalled by Wise Pharmacy...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Dexamethasone Sodium Phosphate PF 24 mg/mL Injection Recalled by Wise...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Gentamicin (GU) Irrigation 240 mg/500 mL Solution Recalled by Wise Pharmacy...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Alprostadil 100 mcg/mL Injectable Recalled by Wise Pharmacy Due to Lack of...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine/Alprostadil 30 mg/0.2 mg/10 mcg/mL Injectable...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine/Alprostadil 30 mg/2 mg/30 mcg/mL Injectable Recalled...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine/Alprostadil - 30 mg/1 mg/10 mcg/mL Injectable...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Acetylcysteine 2% Otic Drop Recalled by Wise Pharmacy Due to Lack of...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine/Alprostadil 30 mg/2 mg/50 mcg/mL Injectable Recalled...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine/Alprostadil/Atropine 30 mg/2 mg/50 mcg/0.15 mg/mL...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 22, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate 100 test kit-for IVD of folate Recalled by...

The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· GETINGE US SALES LLC

Recalled Item: Getinge MCC Flow i Disposable CO2 absorber Recalled by GETINGE US SALES LLC...

The Issue: Reversed expiration and manufacturing date on the label

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit )- for IVD Recalled by Siemens...

The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· Zeus Scientific, Inc.

Recalled Item: Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay Recalled...

The Issue: Assay files used on the open Dynex DSX Instrument to process IVD ELISA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit)-for IVD of folate Recalled by...

The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· DeRoyal Industries Inc

Recalled Item: DeRoyal Enteral Safe Feeding Tubes: a) Recalled by DeRoyal Industries Inc...

The Issue: Certain MED-RX Polyurethane Feeding Tubes are being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Philips North America, LLC

Recalled Item: Philips 5-Lead Set Recalled by Philips North America, LLC Due to The...

The Issue: The thickness of the connector to the trunk cable on affected limb lead sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...

The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 19, 2019· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm FDR Go Plus mobile X-ray system Recalled by Fujifilm Medical...

The Issue: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue...

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

Class II — Potential Health HazardOngoing