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. 2,692 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,692 in last 12 months

Showing 2404124060 of 55,713 recalls

Medical DeviceApril 29, 2019· Philips North America, LLC

Recalled Item: Philips IntelliBridge System configured with a regional setting which uses...

The Issue: Infusion Pump Data Storage Accuracy-Data from the BBraun Space LAN or...

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

Class III — Low RiskOngoing
Medical DeviceApril 29, 2019· COVIDIEN LLC

Recalled Item: MAHURKAR and Argyle acute hemodialysis catheters Recalled by COVIDIEN LLC...

The Issue: The priming volume values printed on the MAHURKA and Argyle acute catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2019· Philips Ultrasound Inc

Recalled Item: Philips EPIQ and Affiniti Ultrasound Systems with software version 4.0:...

The Issue: There is a potential that the image of one patient could get unexpectedly...

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

Class II — Potential Health HazardOngoing
DrugApril 29, 2019· Pfizer Inc.

Recalled Item: Relpax (eletriptan HBr) 40 mg Recalled by Pfizer Inc. Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength: an artwork error on the...

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

Class III — Low RiskOngoing
Refund
DrugApril 26, 2019· Advanced Pharma Inc.

Recalled Item: HYDROmorphone 20 mg/100 mL Injectable Solution Recalled by Advanced Pharma...

The Issue: Sub-potency

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: SOLOPATH Balloon Expandable TransFemoral System Recalled by Terumo Medical...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: Portico Solo Re-Collapsible Access System Recalled by Terumo Medical...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· PF Consumer Healthcare 1 LLC

Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...

The Issue: There is the potential that a HeatWrap could include cells that have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: SOLOPATH Re-Collapsible Access System Recalled by Terumo Medical Corporation...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· PF Consumer Healthcare 1 LLC

Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...

The Issue: There is the potential that a HeatWrap could include cells that have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Inovo, Inc

Recalled Item: Inovo Single Luman Conserver Product Usage: This device is intended Recalled...

The Issue: The pressure gauge (manometer) may dislodge from the threaded...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Cytocell Ltd.

Recalled Item: Aquarius D13S319 Plus Deletion Probe Recalled by Cytocell Ltd. Due to There...

The Issue: There is an error in the chromomap on the package insert.

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

Class III — Low RiskOngoing
FoodApril 26, 2019· Oregons Wild Harvest Inc

Recalled Item: Dried whole elderberry Recalled by Oregons Wild Harvest Inc Due to Dried...

The Issue: Dried whole Elderberries are recalled due to glass fragments contamination.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 25, 2019· ASTRA, LLC

Recalled Item: Lidar System for Erosion Flume Application Class 1 Laser Product Recalled by...

The Issue: Failure to comply event due to incorrect labeling of a class 1 laser product.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2019· Mako Surgical Corporation

Recalled Item: 2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)...

The Issue: The bearings of the saw attachments were ungreased.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2019· Medline Industries Inc

Recalled Item: Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product...

The Issue: Potential risk of brush detachment during cleaning. If brush detachment is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2019· Mako Surgical Corporation

Recalled Item: 2.7 Degree Straight Sagittal Saw attachment (Mako Total Knee Application...

The Issue: The bearings of the saw attachments were ungreased.

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

Class II — Potential Health HazardOngoing
DrugApril 25, 2019· Advantice Health

Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters...

The Issue: Labeling: Not Elsewhere Classified: Full cases may contain canisters that...

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

Class III — Low RiskOngoing
Refund
DrugApril 25, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Acyclovir Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Labeling;...

The Issue: Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2019· US Worldmeds LLC

Recalled Item: Revonto (dantrolene sodium for injection) Recalled by US Worldmeds LLC Due...

The Issue: Presence of Precipitate: Appearance is Out of Specification for the...

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

Class II — Potential Health HazardOngoing
Refund