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. 1,172 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,172 in last 12 months

Showing 9981–10000 of 30,921 recalls

Medical DeviceMay 27, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS pheno- angiography systems developed for single and biplane diagnostic...

The Issue: Software error VE10B -In case of a fault within the drivetrain of an axis...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Stryker GmbH

Recalled Item: Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a...

The Issue: The devices have a different inner diameter than the diameter specified on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Cytocell Ltd.

Recalled Item: Cytocell LPH019-A E2A (TCF3) Breakapart Probe- In Vitro Diagnostic Analyte...

The Issue: May show unexpected locus specific signals in addition to those at 19p13.3....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Stryker GmbH

Recalled Item: Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a...

The Issue: The devices have a different inner diameter than the diameter specified on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Ion Beam Applications S.A.

Recalled Item: Proteus 235-Proton Therapy System Recalled by Ion Beam Applications S.A. Due...

The Issue: if the user forgets to select the trigger input manually while beam gating...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Philips Healthcare

Recalled Item: Azurion systems with software release R2.0.x Recalled by Philips Healthcare...

The Issue: In the Azurion system, the user can add a new study to a patient by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Owen Mumford USA, Inc.

Recalled Item: Unifine Pentips Plus Recalled by Owen Mumford USA, Inc. Due to Mixed Up. Two...

The Issue: Mixed Up. Two (2) cases of Unifine Pentips Plus 4mm pen needles have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards VAMP Jr. 6 in (15 cm) Recalled by Edwards Lifesciences, LLC Due to...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards Recalled by Edwards Lifesciences, LLC Due to There is a potential...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave (3 cc)/VAMP Jr Recalled by Edwards Lifesciences, LLC Due to...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave (30 cc)/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave 3 cc/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC Due...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave (30 cc)/VAMP Jr/52 in (132 cm) Kit Recalled by Edwards...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit Recalled by Edwards...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit Recalled by Edwards...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Flowonix Medical Inc

Recalled Item: Physician Order Form (PL-15400-00 Recalled by Flowonix Medical Inc Due to...

The Issue: Physician Order Form (PL-15400-00 Nov 2018) distributed is discontinued due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion systems with software release R1.x Recalled by PHILIPS MEDICAL...

The Issue: In the Azurion system, the user can add a new study to a patient by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2021· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus Pro - Patient physiological monitor Recalled by Remote Diagnostic...

The Issue: The Tempus Pro (Trizeps 7 only) when used in combination with a specified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2021· Medline Industries Inc

Recalled Item: Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Recalled...

The Issue: Potential for mold contamination (Aspergillus vadensis)

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Titan 3T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing