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. 2,585 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,585 in last 12 months

Showing 4638146400 of 55,713 recalls

Medical DeviceJune 23, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: BD Vacutainer SST Tubes (RED/GREY TOP SST TUBE 3.5ML) Part Recalled by...

The Issue: Products were held at improper storage temperature

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: BD Vacutainer PST Tubes (GOLD TOP PST TUBE 3ml) Part Recalled by Fresenius...

The Issue: Products were held at improper storage temperature

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: BD Vacutainer Citrate Tubes (LIGHT BLUE TOP TUBE 2.7ML)Part number: Recalled...

The Issue: Products were held at improper storage temperature

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: BD Vacutainer EDTA Tubes (LAVENDER TOP TUBE 2.0ML) Part Number: Recalled by...

The Issue: Products were held at improper storage temperature

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: BD Vacutainer Trace Element Tubes (ROYAL BLUE TOP TUBE 6.0ML) Recalled by...

The Issue: Products were held at improper storage temperature

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: BD Vacutainer Serum Tubes (RED TOP PLAIN TUBE 6.0 ML)Part Recalled by...

The Issue: Products were held at improper storage temperature

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Cordis Corporation

Recalled Item: Cordis EMPIRA NC RX PTCA Dilatation Catheter Recalled by Cordis Corporation...

The Issue: The balloon may exhibit resistance to the removal of the balloon cover....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Cordis Corporation

Recalled Item: Cordis EMPIRA RX PTCA Dilatation Catheter Recalled by Cordis Corporation Due...

The Issue: The balloon may exhibit resistance to the removal of the balloon cover....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT: product code 882482 Recalled by Philips Medical Systems...

The Issue: Flat Panel Display (FPD) failed to remain securely locked in the deployed...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2014· Novel Laboratories, Inc.

Recalled Item: Famotidine for Oral Suspension Recalled by Novel Laboratories, Inc. Due to...

The Issue: Failed Impurity/Degradation Specification; 12-month stability time point

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

Class III — Low RiskOngoing
Refund
DrugJune 20, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Tolterodine Tartrate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; Out of specification for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 20, 2014· Stryker Endoscopy

Recalled Item: Disposable StrykeFlow Tip Recalled by Stryker Endoscopy Due to Internal...

The Issue: Internal review found that six lots of Disposable StrykeFlow Tips were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· Laser Peripherals LLC

Recalled Item: LP Recalled by Laser Peripherals LLC Due to Mislabeling

The Issue: Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· ORIGIO, Inc

Recalled Item: Name: Pasteur Pipets Recalled by ORIGIO, Inc Due to Identification of...

The Issue: Identification of packaging breach of the nylon pouch sterile barrier for...

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

Class II — Potential Health HazardOngoing
DrugJune 19, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Mckesson Packaging Services

Recalled Item: Aspirin DR Enteric Coated Tablets Recalled by Mckesson Packaging Services...

The Issue: Failed Dissolution Specification; at the 12 month time interval.

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Pfizer Inc.

Recalled Item: Cardura XL (doxazosin mesylate extended release tablets Recalled by Pfizer...

The Issue: Failed Impurities/Degradation Specifications: Product from this lot may not...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Forest Pharmaceuticals Inc

Recalled Item: Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to...

The Issue: Failed Dissolution Specifications: Drug failed stage III dissolution testing.

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

Class II — Potential Health HazardOngoing
Refund