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. 1,142 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,142 in last 12 months

Showing 13761–13780 of 30,921 recalls

Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S8-3t UDI (01)00884838073524 Can be used as Recalled by Philips...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S7-3t UDI (01)00884838067530 Used as accessory with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Central Recalled by Spacelabs Healthcare, Inc. Due to The firm...

The Issue: The firm received reports of loss of audio alarm after a power failure or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2019· LABSTYLE INNOVATIONS

Recalled Item: Dario Blood Glucose Monitoring System Recalled by LABSTYLE INNOVATIONS Due...

The Issue: The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...

The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...

The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...

The Issue: A mismatch between the angle of the hole in the base and the angle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...

The Issue: A mismatch between the angle of the hole in the base and the angle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Drill Sleeve Guides Recalled by Ad-Tech Medical Instrument...

The Issue: The inner diameter of the drill sleeve guide raw material was found to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz Recalled by Karl Storz Endoscopy Due to During a complaint...

The Issue: During a complaint investigation it was determined that an error was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz NEURO-FIBERSCOPE Recalled by Karl Storz Endoscopy Due to During a...

The Issue: During a complaint investigation it was determined that an error was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE Recalled by Karl Storz Endoscopy...

The Issue: During a complaint investigation it was determined that an error was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2019· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...

The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2019· LivaNova Deutschland GmbH

Recalled Item: Control Panel 60-02-50: LivaNova SCP Pump Control Panel Recalled by LivaNova...

The Issue: The SCP control Panel rotary knob used to control rotary speed of the pump...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2019· LivaNova Deutschland GmbH

Recalled Item: Control Panel 60-02-15: LivaNova SCP Pump Control Panel. Recalled by...

The Issue: The SCP control Panel rotary knob used to control rotary speed of the pump...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2019· Ra Medical Systems, Inc.

Recalled Item: Pharos Excimer Laser Recalled by Ra Medical Systems, Inc. Due to At doses of...

The Issue: At doses of less than 100 mJ, in custom and auto repeat modes, a software...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2019· Philips North America, LLC

Recalled Item: IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The...

The Issue: Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2019· LivaNova USA Inc

Recalled Item: VNS Therapy Recalled by LivaNova USA Inc Due to Sentiva generators may reset...

The Issue: Sentiva generators may reset and become disabled within 60 days of enabling....

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 22, 2019· Thoratec Switzerland GMBH

Recalled Item: CentriMag Acute Circulatory Support System Motor Recalled by Thoratec...

The Issue: Reports have been received of the CentriMag Systems experiencing motor and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 22, 2019· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Concerto & Basic Shower Trolly Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o....

The Issue: The firm has become aware that any of the 4 safety catches may exhibit a...

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

Class II — Potential Health HazardOngoing